TAT: 12-16 weeks price: $1,880.00
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy, NGS Panel (50 genes) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands |
TAT: 4-8 weeks price: $1,545.00
Analysis MYH7 gene (Familial Hypertrophic Cardiomyopathy, Dilated Cardiomyopathy, Non Compaction Cardiomyopathy) method(s): ◦ Sequencing, Capillary (Sanger) Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands |
Hypertrophic Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA |
Left Ventricular Noncompaction Panel method(s): ◦ Sequencing, Next Gen Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA |
DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine - Cambridge, MA, USA |
Pan Cardiomyopathy Panel (62 Genes) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine - Cambridge, MA, USA |
Hypertrophic Cardiomyopathy Panel (20 Genes) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine - Cambridge, MA, USA |
Dilated Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen ApolloGen, Inc. - Irvine, CA, USA |
Hypertrophic Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen ApolloGen, Inc. - Irvine, CA, USA |
Comprehensive Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen ApolloGen, Inc. - Irvine, CA, USA |
iGene Cardiac Panel method(s): ◦ Sequencing, Next Gen ApolloGen, Inc. - Irvine, CA, USA |
iGene Comprehensive Panel (Cancer, Cardiac, Drug Sensitivity) method(s): ◦ Sequencing, Next Gen ApolloGen, Inc. - Irvine, CA, USA |
MYH7-Related Congenital Fiber-Type Disproportion method(s): ◦ Sequencing, Capillary (Sanger) MVZ Dortmund Dr. Eberhard and Partner - Dortmund, Germany |
Cardiomyopathy: Sequencing and Deletion/Duplication Panel method(s): Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Hypertropic Cardiomyopathy: Sequencing and Deletion/Duplication Panel method(s): Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Dilated Cardiomyopathy: Sequencing and Deletion/Duplication Panel method(s): Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
Expanded Neuromuscular Disorders: Sequencing and Deletion/Duplication Panel method(s): Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA |
NGS of 8 genes: ACTC1, DTNA, LDB3, MYBPC3, MYH7, TAZ TNNT2, TPM1. method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS and Sanger Sequencing of the MYH7 gene method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Mutation Scanning of Entire Coding Region Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 13 genes: ACTC1, GLA, LAMP2, LDB3, MYBPC3, MYH7, MYL2, MYL3, PRKAG2, TNNC1, TNNI3, TNNT2, TPM1 method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 13 genes, ACTC1, GLA, LAMP2, LDB3, MYBPC3, MYH7, MYL2, MYL3, PRKAG2, TNNC1, TNNI3, TNNT2, TPM1, and detections of deletions and/or duplications in the GLA, MYBPC3 and TNNT2 genes by MLPA method(s): ◦ Del/Dup (CNV) ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 90 genes: PSEN1, PSEN2, PTPN11, RAF1, RBM20, RPSA, RYR2, SCN5A, SDHA, SGCD, SHOC2, SLC25A4, SOS1, SPRED1, SYNE1, SYNE2, TAZ, TCAP, TGFB3, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL ABCC9, ACTC1, ACTN2, ADRB1, ADRB2, ADRB3, AGL, ANK2, AN method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 34 genes: ACT A1, ATP2A1, BAG3, BIN1, CAV3, CFL2, CLCN1, CNTN1, COL6A1, COL6A2, COL6A3, CRYAB, DES, DNM2, DYSF, FH L1, FLNC, GNE, ISCU, KBTBD13, LDB3, MATR3, MTM1, M YH2, MYH7, MYOT, NEB, RYR1, SEPN1, TNNT1, TPM2, TP M3, TTN, VCP method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 6 genes: COL9 A3, GSN, HSPG2, MYH7, OPA1, TAZ. method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 6 genes: CAV3 , DYSF, FLNC, GNE, MATR3, MYH7. method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 6 genes: GNE, ISCU, MYH2, MYH7, MYOT, VCP method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 154 genes, ABCA1, ABCC6, ABCC9, ACTA2, HRAS, ILK, JPH2, JUP, KCNA5, KCND3, KCNE1, KCNE1L, KCNE2, KCNE3, KCNE4, KCNH2, KCNJ11, KCNJ12, KCNJ2, KCNJ3, KCNJ5, KCNJ8, KCNQ1, KCNQ2, KRAS, LAMA4, LAMP2, LDB3, LDLR, LMNA, LPL, LRP6, MAP2K1, MAP2K2, MEF2A.. method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 8 genes: ACTC1, DES, MYH7, MYPN, TNNI3, TNNT2, TNNC1, TTR method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 44 genes: ABCC9, ACTC1, ACTN2, ADRB1, ADRB2, ADRB3, ANKRD1, BAG3, CRYAB, CSRP3, CTF1, DES, DMD, DSG2, EYA4, FHL2, FKTN, FKRP, ILK, LAMA4, LDB3, LMNA, MYBPC3, MYH6, MYH7, MYPN, NEBL, NEXN, PLN, PSEN1, PSEN2, RBM20, SCN5A, SDHA, SGCD, TAZ, TCAP, TMPO method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 44 genes: ABCC9, ACTC1, ACTN2, ADRB1, ADRB2, ADRB3, ANKRD1, BAG3, CRYAB, CSRP3, CTF1, DES, DMD, DSG2, EYA4, FHL2, FKTN, FKRP, ILK, LAMA4, LDB3, LMNA, MYBPC3, MYH6, MYH7, MYPN, NEBL, NEXN, PLN, PSEN1, PSEN2, RBM20, SCN5A, SDHA, SGCD, TAZ, TCAP, TMPO method(s): ◦ Del/Dup (CNV) ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 35 genes: ACTC1, ACTN2, AGL, ANK2, ANKRD1, CALR3, CAV3, CSRP3, FXN, GAA, GLA, JPH2, LAMP2, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PDLIM3, PLEC, PLN, PRKAG2, SLC25A4, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL and detection of method(s): ◦ Del/Dup (CNV) ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
NGS of 35 genes: ACTC1, ACTN2, AGL, ANK2, ANKRD1, CALR3, CAV3, CSRP3, FXN, GAA, GLA, JPH2, LAMP2, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, MYPN, NEXN, PDLIM3, PLEC, PLN, PRKAG2, SLC25A4, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL. method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain |
Congenital Myopathy Sequencing Panel method(s): ◦ Sequencing, Next Gen University of Chicago, Genetic Services Laboratory - Chicago, IL, USA |
Congenital Myopathy Deletion / Duplication Panel method(s): ◦ Del/Dup (CNV) University of Chicago, Genetic Services Laboratory - Chicago, IL, USA |
Congenital Myopathy with Prominent Contractures Seq Panel method(s): ◦ Sequencing, Next Gen University of Chicago, Genetic Services Laboratory - Chicago, IL, USA |
Congenital Myopathy with Prominent Contractures Del/Dup Panel method(s): ◦ Del/Dup (CNV) University of Chicago, Genetic Services Laboratory - Chicago, IL, USA |
Cardiomyopathy (Dilated) Multi-Gene Panels method(s): ◦ Sequencing, Next Gen Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany |
Cardiomyopathy (General) Multi-Gene Panels method(s): ◦ Sequencing, Next Gen Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany |
Cardiomyopathy (Hypertrophic) Multi-Gene Panels method(s): ◦ Sequencing, Next Gen Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany |
MYH7 Gene Sequencing method(s): ◦ Sequencing, Capillary (Sanger) Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany |
Paediatric Cardiomyopathy NGS Panel method(s): ◦ Sequencing, Next Gen Bristol Genetics Laboratory - Bristol, United Kingdom |
Cardiomyopathies Del/Dup Panel method(s): ◦ Del/Dup (CNV) GeneDx - Gaithersburg, MD, USA |
DCM/LVNC Sequencing Panel method(s): ◦ Sequencing, Next Gen GeneDx - Gaithersburg, MD, USA |
HCM Sequencing Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen GeneDx - Gaithersburg, MD, USA |
Comprehensive Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen GeneDx - Gaithersburg, MD, USA |
Dilated Cardiomyopathy method(s): ◦ Sequencing, Capillary (Sanger) Laboratories AGEL a.s. - Novy Jicin, Czech Republic |
Hypertrophic Cardiomyopathy method(s): ◦ Sequencing, Capillary (Sanger) Laboratories AGEL a.s. - Novy Jicin, Czech Republic |
Congenital Myopathy method(s): ◦ Sequencing, Capillary (Sanger) Cologne University, Institute of Human Genetics - Cologne, Germany |
Familial Hypertrophic Cardiomyopathy, Panel Massive Sequencing (NGS) 40 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Familial Hypertrophic Cardiomyopathy , Sequencing MYH7 Gene method(s): ◦ Sequencing, Capillary (Sanger) Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Dilated Cardiomyopathy, Sequencing MYH7 Gene method(s): ◦ Sequencing, Capillary (Sanger) Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Dilated Cardiomyopathy, Panel Massive Sequencing (NGS) 32 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Cardiomyopathy and Arrhythmia Panel, Sequencing (85 Genes) and Deletion/Duplication (83 Genes) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen ARUP Laboratories, Molecular Genetics Laboratory - Salt Lake City, UT, USA |
Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen Genomic Laboratory of the DNA Research Center LTD (Centrum Badań DNA sp z o.o.) - Poznań, Poland |
Neuromuscular Diseases Panel method(s): ◦ Sequencing, Next Gen Genomic Laboratory of the DNA Research Center LTD (Centrum Badań DNA sp z o.o.) - Poznań, Poland |
Cardiac Diseases Panel method(s): ◦ Sequencing, Next Gen Genomic Laboratory of the DNA Research Center LTD (Centrum Badań DNA sp z o.o.) - Poznań, Poland |
CardioGene Set method(s): ◦ Sequencing, Next Gen Genomics and Pathology Services, Washington University - St. Louis, MO, USA |
Hypertrophic cardiomyopathy (sequence analysis of MYH7,MYBPC3,TNNT2,TNNI3 and TPM1 genes) method(s): ◦ Sequencing, Capillary (Sanger) CGC Genetics - Porto, Portugal |
Familial hypertrophic cardiomyopathy type 1 (CMH1, sequence analysis of MYH7 gene) method(s): ◦ Sequencing, Next Gen CGC Genetics - Porto, Portugal |
Hypertrophic cardiomyopathy - 22 genes (HCM, NGS panel for ACTC1, CAV3, CSRP3, GLA, LAMP2, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, NEXN, PLN, PRKAG2, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN and VCL genes) method(s): ◦ Sequencing, Next Gen CGC Genetics - Porto, Portugal |
Hypertrophic cardiomyopathy - 10 genes (HCM, NGS panel for ACTC1, CSRP3, MYBPC3, MYH7, MYL2, MYL3, TCAP, TNNI3, TNNT2 and TPM1 genes) method(s): ◦ Sequencing, Next Gen CGC Genetics - Porto, Portugal |
Left ventricular noncompaction (LVNC, NGS panel for ACTC1, CSRP3, DTNA, LDB3, LMNA, MYBPC3, MYH7, PLN, SGCD, TAZ, TCAP, TNNT2 and TPM1 genes) method(s): ◦ Sequencing, Next Gen CGC Genetics - Porto, Portugal |
Dilated cardiomyopathy - 22 genes (CMD, NGS panel for ABCC9, ACTC1, ACTN2, CSRP3, DES, DSG2, LDB3, LMNA, MYBPC3, MYH6, MYH7, NEXN, PLN, RBM20, SGCD, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN and VCL genes) method(s): ◦ Sequencing, Next Gen CGC Genetics - Porto, Portugal |
Dilated cardiomyopathy - 10 genes (CMD, NGS panel for ACTC1, CSRP3, LMNA, MYBPC3, MYH7, PLN, SGCD, TCAP, TNNT2 and TPM1 genes) method(s): ◦ Sequencing, Next Gen CGC Genetics - Porto, Portugal |
Cardiomyopathy, Dilated (DCM) method(s): ◦ Sequencing, Next Gen GENETAQ, Molecular Genetics Centre - Malaga, Spain |
Cardiomyopathy Hypertrophic Panel method(s): ◦ Sequencing, Next Gen GENETAQ, Molecular Genetics Centre - Malaga, Spain |
Cardiomyopathy (41 Gene) Panel method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen All Children's Hospital, Johns Hopkins Medicine, Clinical Molecular Genetics Laboratory - St. Petersburg, FL, USA |
CardioNext -Inherited Cadiovascular Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA |
HCMFirst - Hypertrophic Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA |
HCMNext - Hypertrophic Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA |
DCMNext - Dilated Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA |
CMNext - Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA |
LVNCNext - Left Ventricular Non-Compaction Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA |
Congenital Myopathy method(s): ◦ Sequencing, Next Gen GENETAQ, Molecular Genetics Centre - Malaga, Spain |
Neuromuscular Disorders Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen GeneDx - Gaithersburg, MD, USA |
Hypertrophic Cardiomyopathy Multi-Gene Panel, Blood method(s): ◦ Sequencing, Next Gen Mayo Clinic - Minnesota, Personalized Genomics Laboratory - Rochester, MN, USA |
Dilated Cardiomyopathy Multi-Gene Panel, Blood method(s): ◦ Sequencing, Next Gen Mayo Clinic - Minnesota, Personalized Genomics Laboratory - Rochester, MN, USA |
Comprehensive Cardiomyopathy Multi-Gene Panel, Blood method(s): ◦ Sequencing, Next Gen Mayo Clinic - Minnesota, Personalized Genomics Laboratory - Rochester, MN, USA |
Cardiomyopathy in the Context of Neuromuscular Disease method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Muscle Disease with CNS Involvement method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Childhood: Muscle Weakness with Normal or Slightly Elevated CK / Congenital Myopathies method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Muscle Weakness Manifesting in Adulthood / Limb-Girdle Muscular Dystrophy (AD and AR) method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Muscle Disease with Distal Myopathy method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Cardiomyopathy, Hypertrophic method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Cardiomyopathy, Dilated method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Fetal akinesia / Arthrogryposis Multiplex Congenital (AMC) method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Cardiomyopathies, Comprehensive Diagnostics method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Muscle Weakness (Myopathy, Muscular Dystrophy) method(s): ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
MYH7 method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen MGZ München, Medizinisch Genetisches Zentrum München - München, Germany |
Cardiomyopathy, Dilated Panel method(s): ◦ Sequencing, Next Gen CeGaT GmbH - Tübingen, Germany |
Cardiomyopathy, Hypertrophic Panel method(s): ◦ Sequencing, Next Gen CeGaT GmbH - Tübingen, Germany |
Left Ventricular Noncompaction Cardiomyopathy (LVNC) Panel method(s): ◦ Sequencing, Next Gen CeGaT GmbH - Tübingen, Germany |
Congenital Heart Defects Panel method(s): ◦ Sequencing, Next Gen CeGaT GmbH - Tübingen, Germany |
Congenital and Distal Myopathies Panel method(s): ◦ Sequencing, Next Gen CeGaT GmbH - Tübingen, Germany |
Cardiomyopathy Gene Set method(s): ◦ Sequencing, Next Gen Genomics and Pathology Services, Washington University - St. Louis, MO, USA |
Dilated Cardiomyopathy (DCM) Gene Set method(s): ◦ Sequencing, Next Gen Genomics and Pathology Services, Washington University - St. Louis, MO, USA |
Hypertrophic Cardiomyopathy (HCM) Gene Set method(s): ◦ Sequencing, Next Gen Genomics and Pathology Services, Washington University - St. Louis, MO, USA |
Left Ventricular Noncompaction (LVNC) Gene Set method(s): ◦ Sequencing, Next Gen Genomics and Pathology Services, Washington University - St. Louis, MO, USA |
Cardiomyopathy, Restrictive Panel method(s): ◦ Sequencing, Next Gen CeGaT GmbH - Tübingen, Germany |
Cardiomyopathy and changes in cardiac conduction (NGS panel of 59 genes) method(s): ◦ Sequencing, Next Gen CGC Genetics - Porto, Portugal |
Cardiomyopathy (hypertrophic, dilated and arrhythmogenic right ventricular dysplasia, NGS panel of 36 genes) method(s): ◦ Sequencing, Next Gen CGC Genetics - Porto, Portugal |
Familial dilated cardiomyopathy (sequence analysis of LMNA, exons 13, 16 and 23 of MYH7 gene and exons 9, 10, 13 and 15 of TNNT2 gene) method(s): ◦ Sequencing, Capillary (Sanger) CGC Genetics - Porto, Portugal |
Hypertrophic cardiomyopathy (sequence analysis of the exons 13, 16 and 23 of MYH7 gene, exons 17, 24, 25 and 29 of MYBPC3 gene, exons 9, 14 and 16 of TNNT2 gene and exons 7 and 8 of TNNI3 gene ) method(s): ◦ Sequencing, Capillary (Sanger) CGC Genetics - Porto, Portugal |
Single gene testing MYH7 method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) CeGaT GmbH - Tübingen, Germany |
Non-Compaction Cardiomyopathy NGS Panel method(s): ◦ Sequencing, Next Gen DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA |
Dilated Cardiomyopathy: Sequencing Panel method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Dilated Cardiomyopathy: Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Expanded Neuromuscular Disorders: Sequencing Panel method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Restrictive Cardiomyopathy NGS Panel method(s): ◦ Sequencing, Next Gen DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA |
Hypertrophic Cardiomyopathy NGS Panel method(s): ◦ Sequencing, Next Gen DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA |
Left Ventricular Noncompaction, Panel Massive Sequencing (NGS) 7 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Hypertrophic Cardiomyopathy: Sequencing Panel method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Hypertrophic Cardiomyopathy: Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Cardiomyopathy: Sequencing Panel method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Cardiomyopathy: Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Comprehensive Cardiovascular: Sequencing Panel method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Comprehensive Cardiovascular: Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada |
Cardiomyopathy, hypertrophic method(s): ◦ Sequencing, Capillary (Sanger) Cologne University, Institute of Human Genetics - Cologne, Germany |
Cardiovascular disease panel method(s): ◦ Sequencing, Next Gen Genomic Laboratory of the DNA Research Center LTD (Centrum Badań DNA sp z o.o.) - Poznań, Poland |
Hypertrophic Cardiomyopathy Panel method(s): ◦ Sequencing, Capillary (Sanger) Cohesion Phenomics, LLC - Spindale, NC, USA |
Muscle disorders panel method(s): ◦ Sequencing, Next Gen Sherbrooke Genomic Medicine - Sherbrooke, Canada |
Hypertrophic Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen Sherbrooke Genomic Medicine - Sherbrooke, Canada |
Familial Cardiomyopathy Full Gene Sequencing Panel (CardioGeneSeq) method(s): ◦ Sequencing, Next Gen Integrated Genetics, Molecular Diagnostic Laboratory - Westborough, MA, USA |
MYH7 Gene Sequencing method(s): ◦ Sequencing, Next Gen DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA |
Familial Atrial Septal Defect, Isolated, Non-Syndromic NGS Panel method(s): ◦ Sequencing, Next Gen DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA |
Neuromuscular Sequencing Panel method(s): ◦ Sequencing, Next Gen University of Chicago, Genetic Services Laboratory - Chicago, IL, USA |
Catecholaminergic Polymorphic Ventricular Tachycardia, Panel Massive Sequencing (NGS) 14 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Congenital Fiber-Type Disproportion Myopathy, Panel Massive Sequencing (NGS) 6 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Dilated Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA |
DCM and DMD related Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA |
Restrictive Cardiomyopathy (RCM) Panel method(s): ◦ Sequencing, Next Gen Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA |
Comprehensive Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen Cincinnati Children's Hospital Medical Center, Heart Institute Diagnostic Lab - Cincinnati, OH, USA |
Congenital Central Core Myopathy, Panel Massive Sequencing (NGS) RYR1, MYH7, SEPN1, TPM3 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Dilated Cardiomyoptahy Test method(s): ◦ Del/Dup (CNV) Children's Hospital of Eastern Ontario, Genetics Diagnostic Laboratory - Ottawa, Canada |
Dilated Cardiomyopathy Test method(s): ◦ Sequencing, Next Gen Children's Hospital of Eastern Ontario, Genetics Diagnostic Laboratory - Ottawa, Canada |
Hypertrophic Cardiomyopathy Test method(s): ◦ Sequencing, Next Gen Children's Hospital of Eastern Ontario, Genetics Diagnostic Laboratory - Ottawa, Canada |
Hypertrophic Cardiomyopathy Test method(s): ◦ Del/Dup (CNV) Children's Hospital of Eastern Ontario, Genetics Diagnostic Laboratory - Ottawa, Canada |
Pan Cardiomyopathy Panel Test method(s): ◦ Sequencing, Next Gen Children's Hospital of Eastern Ontario, Genetics Diagnostic Laboratory - Ottawa, Canada |
Pan Cardiomyopathy Panel Test method(s): ◦ Del/Dup (CNV) Children's Hospital of Eastern Ontario, Genetics Diagnostic Laboratory - Ottawa, Canada |
Comprehensive Cardiomyopathy (NextGen Sequencing Panel and Copy Number Analysis; 131 genes + mtDNA) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA |
Comprehensive Muscular Dystrophy/Myopathy (NextGen Sequencing Panel and Copy Number Analysis; 407 Genes + mtDNA) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA |
Hereditary Cardiac Arrhythmia (NextGen Sequencing Panel and Copy Number Analysis; 57 genes) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA |
Hereditary Ventricular Tachycardia Syndromes (NextGen Sequencing Panel and Copy Number Analysis; 30 genes) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA |
Left Ventricular Noncompaction Cardiomyopathy Syndromes (NextGen Sequencing Panel and Copy Number Analysis; 8 genes) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA |
Hypertrophic Cardiomyopathy method(s): ◦ Sequencing, Next Gen Asper Biotech Ltd., Asper Biotech - Tartu, Estonia |
Cardiology Genetic Panel (Full), Panel Massive Sequencing (NGS) 110 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Dilated Cardiomyopathy NGS Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen Fulgent Diagnostics - Temple City, CA, USA |
Distal Hereditary Myopathy NGS Panel method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Fulgent Diagnostics - Temple City, CA, USA |
Hypertrophic Cardiomyopathy NGS Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen Fulgent Diagnostics - Temple City, CA, USA |
Left Ventricular Noncompaction NGS Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen Fulgent Diagnostics - Temple City, CA, USA |
MYH7 method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Fulgent Diagnostics - Temple City, CA, USA |
Neuromuscular NGS Panel method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Fulgent Diagnostics - Temple City, CA, USA |
Pan-Cardio NGS Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen Fulgent Diagnostics - Temple City, CA, USA |
Sudden Death Syndrome NGS Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen Fulgent Diagnostics - Temple City, CA, USA |
CGC Genetics panel for sudden death – standard method(s): ◦ Sequencing, Next Gen CGC Genetics - Porto, Portugal |
Dilated Cardiomyopathy method(s): ◦ Sequencing, Capillary (Sanger) GenoMed-Diagnosticos de Medicina Molecular, SA - Lisboa, Portugal |
Hypertrophic Cardiomyopathy method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen GenoMed-Diagnosticos de Medicina Molecular, SA - Lisboa, Portugal |
Comprehensive Hereditary Breast-Ovarian Cancer Panel method(s): ◦ Sequencing, Next Gen NeoGenomics Laboratories - Fort Myers, FL, USA |
TAT: 4-6 weeks price: $3,000.00
Comprehensive Cardiomyopathy Cardiac Arrhythmia Exome Panel method(s): ◦ Sequencing, Next Gen UW Medicine Center for Precision Diagnostics Northwest Clinical Genomics Laboratory - Seattle, WA, USA |
TAT: 4-6 weeks price: $2,500.00
Cardiomyopathy Exome Panel method(s): ◦ Sequencing, Next Gen UW Medicine Center for Precision Diagnostics Northwest Clinical Genomics Laboratory - Seattle, WA, USA |
TAT: 3-4 weeks price: $690.00
Hypertrophic Cardiomyopathy and other MYH7-Related Disorders via the MYH7 Gene method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $840.00
Congenital Fiber Type Disproportion Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $1,290.00
Congenital Myopathy Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $840.00
Core Myopathy Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $1,670.00
Dilated Cardiomyopathy Deletion/Duplication panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $1,290.00
Distal Hereditary Myopathy Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $1,290.00
Hypertrophic Cardiomyopathy Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $840.00
Left Ventricular Noncompaction (LVNC) Deletion/Duplication panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-5 weeks price: $990.00
Hypertrophic Cardiomyopathy and other MYH7-Related Disorders via the MYH7 Gene method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-5 weeks price: $1,690.00
Congenital Fiber Type Disproportion Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-5 weeks price: $2,190.00
Congenital Myopathy Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-5 weeks price: $1,790.00
Core Myopathy Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-5 weeks price: $1,890.00
Dilated Cardiomyopathy Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-5 weeks price: $1,690.00
Distal Hereditary Myopathy Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-5 weeks price: $1,770.00
Hypertrophic Cardiomyopathy Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-5 weeks price: $1,540.00
Left Ventricular Noncompaction (LVNC) Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
CustomNext-Cardio method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA |
Cardiomyopathy, dilated (Kardiomyopathie, dilatativ) method(s): ◦ Sequencing, Next Gen Praxis fuer Humangenetik Wien - Vienna, Austria |
Cardiomyopathy, hypertrophic (Kardiomyopathie, hypertroph) method(s): ◦ Sequencing, Next Gen Praxis fuer Humangenetik Wien - Vienna, Austria |
Sudden death (Plötzlicher Herztod) method(s): ◦ Sequencing, Next Gen Praxis fuer Humangenetik Wien - Vienna, Austria |
Muscle Polyneuropathies, Panel Massive Sequencing (NGS) 112 Genes method(s): ◦ Sequencing, Next Gen Reference Laboratory Genetics - Hospitalet de Llobregat, Spain |
Congenital Myopathies (NextGen Sequencing Panel and Copy Number Analysis; 29 Genes) method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA |
TAT: 3-5 weeks price: $2,490.00
Comprehensive Neuromuscular Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $1,990.00
Comprehensive Neuromuscular Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
Myopathy, distal type 1 method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Centogene AG, Rare Disease Company - Rostock, Germany |
Myosin storage myopathy method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Centogene AG, Rare Disease Company - Rostock, Germany |
Scapuloperoneal myopathy, MYH7 related method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Centogene AG, Rare Disease Company - Rostock, Germany |
Cardiomyopathy, familial hypertrophic type 1 method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Centogene AG, Rare Disease Company - Rostock, Germany |
Cardiomyopathy, dilated type 1S method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Centogene AG, Rare Disease Company - Rostock, Germany |
Cardiomyopathy dilated panel method(s): ◦ Del/Dup (CNV) ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Centogene AG, Rare Disease Company - Rostock, Germany |
Cardiomyopathy hypertrophic panel method(s): ◦ Del/Dup (CNV) ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Next Gen Centogene AG, Rare Disease Company - Rostock, Germany |
Congenital Myopathy Spotlight Panel method(s): ◦ Sequencing, Next Gen Courtagen Life Sciences, Courtagen Diagnostics Laboratory - Woburn, MA, USA |
Distal Myopathy Spotlight Panel method(s): ◦ Sequencing, Next Gen Courtagen Life Sciences, Courtagen Diagnostics Laboratory - Woburn, MA, USA |
Phosphorus Dilated Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Phosphorus Diagnostics - Livingston, NJ, USA |
Phosphorus Hypertrophic Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Phosphorus Diagnostics - Livingston, NJ, USA |
Phosphorus Left Ventricular Noncompaction Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Phosphorus Diagnostics - Livingston, NJ, USA |
Phosphorus Restrictive Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Phosphorus Diagnostics - Livingston, NJ, USA |
Phosphorus Pan Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Phosphorus Diagnostics - Livingston, NJ, USA |
Phosphorus Pan Arrhythmia and Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Phosphorus Diagnostics - Livingston, NJ, USA |
Congenital myopathy panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Centogene AG, Rare Disease Company - Rostock, Germany |
General Cardiomyopathy - 92 gene NGS panel method(s): ◦ Sequencing, Next Gen Clinical Genetics & Genomics Laboratory - London, United Kingdom |
Dilated Cardiomyopathy (DCM) - 59 gene NGS panel method(s): ◦ Sequencing, Next Gen Clinical Genetics & Genomics Laboratory - London, United Kingdom |
Hypertrophic Cardiomyopathy (HCM) - 47 gene NGS panel method(s): ◦ Sequencing, Next Gen Clinical Genetics & Genomics Laboratory - London, United Kingdom |
Non-compaction cardiomyopathy (LVNC) - 10 gene NGS panel method(s): ◦ Sequencing, Next Gen Clinical Genetics & Genomics Laboratory - London, United Kingdom |
Restrictive cardiomyopathy (RCM) - 9 gene panel method(s): ◦ Sequencing, Next Gen Clinical Genetics & Genomics Laboratory - London, United Kingdom |
NGS Neuromuscular Disorders Panel method(s): ◦ Sequencing, Next Gen Greenwood Genetic Center Diagnostic Laboratories - Greenwood, SC, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Left Ventricular Noncompaction Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Hypertrophic Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Cardiomyopathy and Skeletal Muscle Disease Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Dilated Cardiomyopathy Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Congenital Myopathy Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Distal Myopathy Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Comprehensive Myopathy Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Congenital Fiber-Type Disproportion Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Cardiomyopathy Comprehensive Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
TAT: 1-3 weeks price: $1,500.00
Invitae Comprehensive Neuromuscular Disorders Panel method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) Invitae - San Francisco, CA, USA |
Neuromuscular Comprehensive Panel method(s): ◦ Sequencing, Next Gen Courtagen Life Sciences, Courtagen Diagnostics Laboratory - Woburn, MA, USA |
TAT: 3-5 weeks price: $2,400.00
Comprehensive Cardiology Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
Comprehensive Cardiology Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
Congenital Myopathy with Fiber-Type Disproportion Sequencing Panel method(s): ◦ Sequencing, Next Gen University of Chicago, Genetic Services Laboratory - Chicago, IL, USA |
TAT: 3-4 weeks price: $2,630.00
Distal Myopathy NGS Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Connective Tissue Gene Tests - Allentown, PA, USA |
TAT: 3-4 weeks price: $1,630.00
Distal Myopathy NGS Panel method(s): ◦ Sequencing, Next Gen Connective Tissue Gene Tests - Allentown, PA, USA |
TAT: 2-3 weeks price: $1,150.00
Distal Myopathy NGS Panel method(s): ◦ Del/Dup (CNV) Connective Tissue Gene Tests - Allentown, PA, USA |
Comprehensive Cardiology Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
Comprehensive Skeletal / Malformation Syndrome Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
Dilated Cardiomyopathy (DCM) Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
Hypertrophic Cardiomyopathy (HCM) Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
Osteogenesis Imperfecta Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
Comprehensive Cardiology Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
Comprehensive Skeletal / Malformation Syndrome Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
Dilated Cardiomyopathy (DCM) Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
Hypertrophic Cardiomyopathy (HCM) Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
Osteogenesis Imperfecta Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
Cardiomyopathy Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
TAT: 3-5 weeks price: $1,800.00
Sudden Cardiac Arrest Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $1,670.00
Sudden Cardiac Arrest Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
Comprehensive Cardiac Panel method(s): ◦ Sequencing, Next Gen Greenwood Genetic Center Diagnostic Laboratories - Greenwood, SC, USA |
TAT: 3-5 weeks price: $1,980.00
Pan Cardiomyopathy Sequencing Panel method(s): ◦ Sequencing, Next Gen PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |
TAT: 3-4 weeks price: $1,670.00
Pan Cardiomyopathy Deletion/Duplication Panel method(s): ◦ Del/Dup (CNV) PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA |