Cytogenetic Tests

1 2 3 4 5 6 8 9 A B C D E F G H I J K L M N O P R S T U V W X Y

 

1 

10p13-p14 Deletion Syndrome Test
11;14 translocation; t(11;14)(q13;q32) BCL1(CCND1)/IGH
11;18 translocation; t(11;18)(q21;q21) BIRC3/MALT1
11q22 deletion; del(11q22.3) ATM
11q23 KMT2A (MLL)
11q23 MLL rearragements
12;21 translocation, t(12;21)(p12;q2) TEL(ETV6)/AML1(RUNX1)
14q32 IGH
15q11-q13 Duplication Syndrome Test
16p11.2 Microdeletion Test
1p/1q; 1p deletion / 1q amplification
1p32 deletion; del(1p32) SIL-TAL1
1p36 Deletion Syndrome
1p36 Deletion Syndrome Test
1q21.1 Deletion/Duplication Analysis
 

2 

22q11.2 Deletion Syndrome Test
22q11.2 Duplication Test
2p23 inversion; t(2p23) ALK rearragements - Lung Cancer (NSCLC)
 

3 

3;14 translocation, t(3;14)(q27;q32) IGH/BCL6 - Non-Hodgkin Lymphoma
3q29 Deletion Syndrome Test
 

4 

46,XX Testicular Disorder of Sex Development Test
4q12 deletion; del(4q12) FIP1L1/PDGFRa
 

5 

5;14 translocation, t(5;14)(q35;q32) TLX3/BCL11B
5q deletion; -5/del(5q) D5S630/EGR1
5q22 Deletion Syndrome Test
 

6 

6q23 deletion; del(6q23) MYB
 

8 

8, Chromosome 8 trisomy, +8
8;14 translocation; t(8;14)(q24;q32) IGH/MYC
8;21 translocation; t(8;21)(q21.3;q22) RUNX1/RUNX1T1
8p11 rearragements FGFR1 - Myeloproliferative syndrome
8q24 cMYC
 

9 

9;14 translocation; t(9;14)(p13;q32) PAX5/IGH
9;22 translocation; t(9;22)(q34;q11) ABL1/BCR
 

A 

Alagille Syndrome: JAG1 (20p12)
ALK (2p23) Mutations
ALK Gene Rearrangements - Lung Cancer (NSCLC)
Amniotic Karyotype
Analysis of Abortion Material
Analysis of Angelman Syndrome; AS
Analysis of Chromosome 1p36 Deletion Syndrome
Analysis of Chromosome 22q11.2 Duplication Syndrome
Analysis of Cri-Du-Chat Syndrome
Analysis of Developmental Disorders and Mental Retardation
Analysis of Digeorge Syndrome; DGS
Analysis of Diplo-Y Syndrome (47,XYY Syndrome)
Analysis of Down Syndrome (Trisomy 21)
Analysis of Edwards Syndrome (Trisomy 18)
Analysis of Juvenile Myelomonocytic Leukemia; JMML
Analysis of Klinefelter Syndrome (47,XXY Syndrome)
Analysis of Leukemia, Acute Myeloid;
Analysis of Macroglobulinemia, Waldenstrom, Susceptibility To, 1; WM1
Analysis of Miller-Dieker Lissencephaly Syndrome; MDLS
Analysis of Neurofibromatosis, Type I; NF1
Analysis of Patau Syndrome (Trisomy 13)
Analysis of Phelan-Mcdermid Syndrome
Analysis of Prader-Willi Syndrome; PWS
Analysis of Silver-Russell Syndrome; SRS
Analysis of Smith-Magenis Syndrome; SMS
Analysis of Triple X Syndrome (47,XXX Syndrome)
Analysis of Ullrich-Turner Syndrome (45,X)
Analysis of Velocardiofacial Syndrome
Analysis of Williams-Beuren Syndrome; WBS
Analysis of Wolf-Hirschhorn Syndrome (del 4p)
Aneuploidy FISH Panel
Aneuploidy Screening with Rapid FISH
Aneupolidy Screen
Angelman Syndrome
Angelman Syndrome Test
Angelman Syndrome, FISH Prenatal Diagnostic
Angelman Syndrome, FISH Whole Blood
ANOS1 FISH
ANOS1 Gene Sequencing and FISH
Array SNP-Based Analysis
Ataxia-Telangiectasia
Ataxia-Telangiectasia Test
Autism Panel: Complete Tier 1
Autism Panel: Tier 1 Cytogenetic and Molecular
Autism Spectrum Disorders Test
 

B 

Beckwith-Wiedemann Syndrome Test
Blood chromosome analysis
Blood Karyotype
Bloom Syndrome
Bloom Syndrome Test
Bone Marrow for Karyotyping Leukemia
Brain Malformations: Deletion/Duplication Panel
 

C 

C-MET Protooncogene, FISH Tissue
Carney Complex
CEN6/6q21/6q23
Charcot-Marie-Tooth Neuropathy Type 1A Test
CHARGE Syndrome Test
Chorionic Villus, FISH
Chromosomal CGH Microarray: Prenatal testing
Chromosomal microarray (array CGH, Cytoscan 750K)
Chromosomal Microarray (CMA)
Chromosomal microarray 60K probes
Chromosomal microarray analysis (array CGH, Cytoscan HD)
Chromosomal Microarray Analysis - Comprehensive
Chromosomal Microarray: CGH
Chromosomal Microarray: CytoScan SNP Array
Chromosomal Microarray: CytoScan SNP Array Oncology
Chromosomal Microarray: CytoScan SNP Array POC
Chromosomal Microarray: CytoScan SNP Array Prenatal
Chromosomal Microarray: EmArray Cyto
Chromosomal Microarray: EmArray Cyto Prenatal
Chromosomal microarray: hematological disorders and malignancies
Chromosomal Microarray: SNP
Chromosomal Microarray; Constitutional
Chromosomal SNP Microarray (CMA)
Chromosomal SNP Microarray: Prenatal testing
Chromosomal SNP Microarray: Products of conception – Prenatal testing
CHROMOSOME 21
Chromosome Analysis
Chromosome Analysis - Blood - High Resolution
Chromosome Analysis - Prenatal - Amniotic Fluid
Chromosome Analysis - Prenatal - Amniotic Fluid with ACHE
Chromosome Analysis - Prenatal - Amniotic Fluid with AFP
Chromosome Analysis - Prenatal - Amniotic Fluid with AFP, ACHE, and FH
Chromosome Analysis - Prenatal - CVS
Chromosome Analysis by G-banding
Chromosome Analysis from Skin Biopsy
Chromosome Analysis from Solid Tissue Material
Chromosome Analysis in Abortion/Miscarriage Material
Chromosome Analysis in Amniotic Fluid
Chromosome Analysis in Amniotic Fluid with Rapid FISH Result
Chromosome Analysis in Amniotic Fluid with Rapid QF-PCR Result
Chromosome Analysis in Bone Marrow Aspiration Material
Chromosome Analysis in Chorionic villus sampling (CVS)
Chromosome Analysis in Fetal Blood
Chromosome Analysis in Peripheral Blood
Chromosome Analysis in Peripheral Blood (Leukemia)
Chromosome analysis of amniotic fluid
Chromosome analysis of chorionic villi
Chromosome analysis of non-stimulated cultures (bone marrow and/or blood)
Chromosome analysis of stimulated cultures (blood)
Chromosome analysis of stimulated cultures (fetal blood)
Chromosome analysis of tissue fibroblasts
Chromosome Analysis with Karyotyping
Chromosome Analysis, Amniotic Fluid
Chromosome Analysis, Amniotic Fluid, with Reflex to Genomic Microarray
Chromosome Analysis, Chorionic Villi
Chromosome Analysis, Chorionic Villus
Chromosome Analysis, Chorionic Villus Sample (CVS)
Chromosome Analysis, Peripheral Blood
Chromosome Analysis, Peripheral Blood (routine)
Chromosome Analysis, Peripheral Blood (rule out Mosaicism)
Chromosome Analysis, Peripheral Blood,
Chromosome Analysis, Peripheral Blood, with Reflex to Genomic Microarray
Chromosome Analysis, Products of Coception (POC)
Chromosome Analysis, Products of Conception
Chromosome Analysis, Products of Conception, with Reflex to Genomic Microarray
Chromosome Analysis, PUBS
Chromosome Analysis, Rule Out Mosaicism
Chromosome Analysis, Skin Biopsy
Chromosome Analysis: Amniotic Fluid
Chromosome Analysis: Chorionic Villi
Chromosome Analysis: Fetal Blood (Percutaneous Umbilical Blood Sampling/PUBS)
Chromosome Analysis: Peripheral Blood (Age: 6 months and above)
Chromosome Analysis: Peripheral Blood (Age: Less than 6mo)
Chromosome Analysis: Peripheral Blood (Mosaicism)
Chromosome Analysis: Products of Conception (POC)
Chromosome Analysis: Skin/Other Tissue
Chromosome Analysis: Targeted Family Member Study
Chromosome Breakage Analysis
Chromosome breakage analysis, prenatal
Chromosome breakage studies for Fanconi's anaemia
Chromosome FISH
Chromosome FISH, Amniotic Fluid with Reflex to Chromosome Analysis or Genomic Microarray
Chromosome FISH, Chorionic Villus with Reflex to Chromosome Analysis or Genomic Microarray
Chromosome FISH, Metaphase
Chromosome FISH, Prenatal
Chromosome Microarray Analysis
CHROMOSOMES 13, 18, 21, X and Y
CHROMOSOMES 13, 21
CHROMOSOMES 18, X and Y
ClariView Array (Microarray)
CMA-Expanded and Limited Karyotype-Amniotic Fluid
CMA-Expanded and Limited Karyotype-CVS
CMA-Targeted and Limited Karyotype-Amniotic Fluid
CMA-Targeted and Limited Karyotype-CVS
Com.Pl.i.t. DX 54 genes - Comprehensive Panel for Individualized Cancer Threatment
Comprehensive Fetal and Neonatal Loss Panel
Constitutional Cytogenomic Microarray Analysis
CREBBP Gene (Karyotyping and FISH)
CREBBP-Related Rubinstein-Taybi Syndrome Test
Cri du Chat Syndrome Test
Cri du Chat Syndrome, FISH Prenatal Diagnosis
Cri du Chat Syndrome, FISH Whole Blood
Cri-du-Chat syndrome (5p15 deletion)
Cri-du-chat Syndrome (FISH)
Cytogenetic analysis on digital images (acquired disease)
Cytogenetic analysis on digital images (fibroblasts)
Cytogenetic analysis on digital images (lymphocytes)
Cytogenetic diagnostics
Cytogenomic Molecular Inversion Probe Array, FFPE Tissue - Products of Conception
Cytogenomic SNP Microarray
Cytogenomic SNP Microarray - Fetal
Cytogenomic SNP Microarray with Five-Cell Chromosome Study, Peripheral Blood
Cytogenomic SNP Microarray, Buccal Swab
CytoScan HD Microarray Test
CytoScan® Dx (FDA-Cleared) Microarray Test
 

D 

DEB Test
del(11q) ATM
del(13)(q14)
del(17p) TP53
Detection by FISH of 1p36/1q25
Detection by FISH of 1q+
Detection by FISH of 22q11.2 delection
Detection by FISH of 5q31 deletion (EGR1 gene)
Detection by FISH of aneuploidies in sperm (5 probes)
Detection by FISH of aneuploidies in sperm (7 probes)
Detection by FISH of aneuploidies in sperm (9 probes)
Detection by FISH of cen 13/21
Detection by FISH of Cri-du-chat syndrome
Detection by FISH of Down syndrome
Detection by FISH of EGFR
Detection by FISH of HER2
Detection by FISH of IGH
Detection by FISH of Miller-Dieker syndrome
Detection by FISH of PDGFRB (5q32) rearrangements
Detection by FISH of Phelan-McDermid syndrome
Detection by FISH of Prader-Willi/Angelman syndromes (15q11.2)
Detection by FISH of sexual chromosomes (X/SRY)
Detection by FISH of sexual chromosomes (X/Y, centromeric)
Detection by FISH of Smith-Magenis syndrome
Detection by FISH of subtelomeric rearrangements
Detection by FISH of Williams syndrome
Detection by FISH of Wolf-Hirschhorn syndrome
DGS/VCFS Deletion FISH Analysis
Di George Syndrome , FISH Whole Blood
Di George Syndrome, FISH Prenatal Diagnostic
Di-George Syndrome
Di-George/Velocardiofacial syndrome (22q11 microdeletion)
Digeorge Syndrome (FISH)
DiGeorge Syndrome I (22q only)
DIH1-Related Congenital Diaphragmatic Hernia Test
 

E 

EGFR Amplifications
EGFR Gene, FISH Tissue
EGFR Gene, Tissue Screening Mutations
ELN FISH
Endocrine Disorders: Deletion/Duplication Panel
Expanded CMA - Prenatal - Amniotic Fluid
Expanded CMA - Prenatal - CVS
 

F 

Familial Mutation Testing: Targeted Deletions/Duplications
Fanconi Anemia
Fanconi Anemia Test
Female Specific Comprehensive Autism Panel
FISH after Pregnancy Loss
FISH Analysis
FISH Analysis - Prenatal Aneuploidy
FISH analysis of CKS1B/CDKN2C genes amplification/deletion
FISH analysis with centromeric probe
FISH analysis with centromeric probe - chromosome 12
FISH analysis with centromeric probe - chromosome 15
FISH analysis with centromeric probe - chromosome 6
FISH analysis with centromeric probe - chromosome 8
FISH analysis with centromeric probe - chromosome 9
FISH Analysis with Culture
FISH Analysis With One Centromere Probe Or Probe For XY Chromosomes Test
FISH Analysis With One Specific Probe Test
FISH analysis with painting probe
FISH analysis with subtelomeric probe
FISH analysis with unique sequence probe
FISH Analysis without Culture
FISH Analysis: Telomere Panel
FISH for Aneuploidy
FISH for Congenital Aberrations Test
FISH for Prader-Willi/Angelman Syndrome
FISH for Velocardiofacial/DiGeorge/22q11.2 deletion Syndrome and 22q11.2 duplication syndrome
FISH for Williams Syndrome
FISH PANEL-Langer Giedion
FISH PANEL-Multiple Exostoses
FISH PANEL-Velocardiofacial Syndrome
FISH Panel: Aneuploidy (13, 18, 21, X and Y)
FISH test on peripheral Blood/Bone marrow, BCR/ABL or Philadelphia translocation
FISH test on peripheral Blood/Bone marrow, deletion 11q23 or LSIL MLL gene breakapart
FISH test on peripheral Blood/Bone marrow, deletion 13q
FISH test on peripheral Blood/Bone marrow, deletion 14q32.3 or LSI IGH gene breakapart
FISH test on peripheral Blood/Bone marrow, inversion 16 or LSI CBFB
FISH test on peripheral Blood/Bone marrow, Opposite Sex BMT (XX / XY)
FISH test on peripheral Blood/Bone marrow, t(11;14) or LSI IGH/CCND1
FISH test on peripheral Blood/Bone marrow, t(12;21) or LSI TEL/AML1
FISH test on peripheral Blood/Bone marrow, t(15;17) or LSI PML/RARA
FISH test on peripheral Blood/Bone marrow, t(8;21) or LSI ETO/AML1
FISH Whole chromosome painting
FISH-1P36 Deletion
FISH-Adrenal Hypoplasia Congenita
FISH-Alagille Syndrome
FISH-Angelman Syndrome
FISH-Beckwith-Wiedemann Syndrome
FISH-Charcot-Marie-Tooth (CMT1A) DI
FISH-Cri du Chat
FISH-Di George Syndrome II (10P ONL
FISH-Glycerol Kinase Deficiency
FISH-Hereditary Neuropathy W/ LIABI
FISH-Isolated Lissencephaly
FISH-Kallman Syndrome
FISH-Microphthalmia with Linear Skin Defects
FISH-Miller-Dieker Syndrome
FISH-Multiple Exostoses 1(EXT1)
FISH-Multiple Exostoses 2/Potocki-Shaffer Syndrome
FISH-Neurofibromatosis 1
FISH-Prader-Willi Syndrome
FISH-Rubinstein-Taybi Syndrome
FISH-Smith-Magenis Syndrome
FISH-Sotos Syndrome
FISH-SRY Analysis
FISH-Trichorhinophalangeal Syndrome
FISH-WAGR Syndrome
FISH-Williams Syndrome
FISH-Wilms Tumor
FISH-Wolf-Hirschhorn Syndrome
FISH-X-Linked Ichthyosis/STS Deficiency
FISH: Williams Syndrome 7q11.23
FISH: 1p36 Deletion Syndrome
FISH: 22q11.2 Deletion Syndrome
FISH: Kallman Syndrome (Xp22.3)
FISH: POC Aneuploidy (X,Y,13,15,16,18,21,22)
FISH: Prader-Willi/Angelman syndrome (15q11-q13)
FISH: Prenatal Panel 13, 18, 21, X and Y
FISH: Steroid Sulfatase Deficiency (Xp22.3)
FISH: X-inactivation (Xist)
FISH: Yp11.3 (SRY detection)
Fragile X Syndrome (Cytogenetics)
 

G 

Genetic Fetal Blood Karyotyping
Genetic High Resolution Karyotyping
Genetic Karyotyping Chromosome Analysis
Genetic m-FISH (Multicolor Fluorescence In-Situ Hybridization)
Genomic SNP Microarray, Products of Conception
 

H 

Hereditary Multiple Osteochondromatosis, Type I Test
Hereditary Multiple Osteochondromatosis, Type II Test
High Resolution Chromosome Analysis
 

I 

i(17q) RARa
Ichthyosis, X-Linked Test
Infertility Panel: Female
Infertility Panel: Male
InSight (Interphase FISH for rapid detection of numerical abnormalities of chromosomes 13, 18, 21, X and Y)
Interphase FISH analysis of fixed material
inv(16) CBFB
Isolated Aniridia Test
Isolated Lissencephaly Sequence
 

J 

Jacobsen Syndrome Test
JAG1-Related Alagille Syndrome Test
 

K 

Kallmann Syndrome 1 Test
KaryoNIM 60K Postnatal
Karyotype from Blood Sample
 

L 

Langer-Giedion Syndrome Test
Leukaemia chromosome analysis
Limb Malformation: Deletion/Duplication Panel
LIS1-Associated Lissencephaly/Subcortical Band Heterotopia Test
Lissencephaly (NGS panel for 12 genes)
Lynch Syndrome Test
 

M 

Male Specific Comprehensive Autism Panel
Marker Chromose Identification
Maternal Uniparental Disomy
MECP2 Duplication Syndrome Test
MECP2-Related Disorders Test
Medical Exome Array: Deletion/Duplication Analysis
Metaphase FISH analysis
Microsatellite Instability
Miller-Diecker Syndrome Test
Miller-Dieker Syndrome
Miller-Dieker Syndrome (FISH)
Miller-Dieker Syndrome, FISH Prenatal Diagnosis
Miller-Dieker Syndrome, FISH Whole Blood
Mircroarray CGH
Miscarriage Sample Analysis Test (X, Y, 13, 18, 21)- FISH
Miscarriage Sample Analysis Test (X, Y, 13, 18, 21, 16)- FISH
Miscarriage Sample Analysis Test (X, Y, 13, 18, 21, 16, 15, 22)-FISH
Miscarriage Sample Analysis Test (X, Y, 13, 18, 21, 16, 22)-FISH
Miscarriage Sample Analysis Test (X, Y, sex identification)-FISH
Mitomycin C Test
Mowat-Wilson Syndrome Test
Multicolor FISH (M-FISH)/Spectral Karyotyping
 

N 

Neoplasia Cytogenomic Microarray Analysis
Neurofibromatosis 1 Test
Neurofibromatosis 2 Test
Nijmegen Breakage Syndrome
Nijmegen Breakage Syndrome Test
 

O 

OncoFISH for AML (7 probes - t(15;17), inv(16), t(8;21), 11q-, 5q-, 7q-, BCL6)
OncoFISH for CLL (6 probes)
OncoFISH for MM (5 probes)
OncoFISH for MM (6 probes)
OncoFISH for ploidy in MM (centromeres 5, 9 and 15)
OncoFISH-R for MM (6 probes)
Optic Atrophy: Deletion/Duplication Panel
 

P 

Pallister-Killian Syndrome Test
Pallister-Killian Syndrome, FISH Prenatal Diagnosis
Pallister-Killian Syndrome, FISH Whole Blood
Paraffin section FISH studies
Phelan-McDermid Syndrome Test
Phelan-McDermid Syndrome, Deletion 22q13.3 (FISH) Prenatal Diagnosis
Phelan-McDermid Syndrome, Deletion 22q13.3 (FISH) Whole Blood
Pompe Disease: GAA Gene Deletion/Duplication
Potocki-Lupski Syndrome Test
Prader-Willi Syndrome
Prader-Willi Syndrome (FISH)
Prader-Willi Syndrome Test
Prader-Willi Syndrome, FISH Prenatal Diagnosis
Prader-Willi Syndrome, FISH Whole Blood
Prenatal Aneuploidy Evaluation (chromosomes 13, 18, 21, X, and Y)
Prenatal chromosome analysis
Prenatal Diagnosis
Prenatal FISH DiGeorge Syndrome
Prenatal Rapid Aneuploidy FISH
Prenatal Rapid Screen by FISH for 13, 18, 21, X and Y
Prenatal SNP Chromosome Microarray
Proportionate Short Stature/Small for Gestational Age: CytoScan SNP Array, Russell-Silver Panel, UPD14 Analysis, Sequencing and Deletion/Duplication Panel
Proportionate Short Stature/Small for Gestational Age: CytoScan SNP Array, Sequencing, and Deletion/Duplication Panel
Proportionate Short Stature/Small for Gestational Age: SNP Array, Russell-Silver Panel, UPD14 Analysis, and Sequencing Panel
PTEN Deletion
 

R 

RAI1 FISH Deletion Analysis
Rapid FISH (Aneuvysion-13, 18, 21, X, Y)
Rapid sex chromosome FISH
Retinoblastoma (RB1 Deletion)
Retinoblastoma , Deletion 13q14 FISH Whole Blood
Retinoblastoma Test
Rhabdoid Tumor Predisposition Syndrome 1 Test
Rubinstein-Taybi Syndrome
Rubinstein-taybi Syndrome (del 16p13.3) FISH
Rubinstein-Taybi Syndrome, FISH Prenatal Diagnosis
Rubinstein-Taybi Syndrome, FISH Whole Blood
 

S 

SCE Test
Schwannomatosis Test
SHOX
SHOX Deletion
SHOX Deletion Test
SHOX-Related Haploinsufficiency Disorders Test
Silver-Russell Syndrome , Uniparental Disomy Chromosome 7 (UPD7)
Single Chromosome Painting (FISH)
Single Chromosome Subtelomeric (FISH)
Smith-Magenis Syndrome
Smith-Magenis Syndrome , FISH Prenatal Diagnosis
Smith-Magenis Syndrome , FISH Whole Blood
Smith-Magenis Syndrome Test
SNP Array
SNP array for Prenatal, Pregnancy Loss and Postnatal diagnosis
SNP Chromosome Microarray-Pediatric
Solid tumour chromosome analysis
Sotos Syndrome
Sotos Syndrome (FISH)
Sotos Syndrome Test
Sperm DNA Damage and Genetic Screening
SRY
SRY (Sex determining Region of Y)
SRY Analysis
SRY Deletion (FISH)
SRY Deletion FISH
SRY-Related 46,XY DSD and 46,XY CGD Test
STAT FISH Chromosome 13
STAT FISH Chromosome 18
STAT FISH Chromosome 21
STAT FISH Chromosomes XandY
STAT FISH: 22q11 Microdeletion
Steroid Sulfatase Deficiency
Steroid Sulfatase Deficiency (FISH)
Subtelomeric Deletion (FISH)
Subtelomeric FISH Screen
Subtelomeric FISH Test
SYP-related XLMR: SYP Gene Deletion/Duplication
 

T 

t(12;21) ETV6/RUNX1 (TEL/AML1)
t(15;17) PML/RARa
t(8;21) RUNXT1/RUNX1 (ETO/AML1)
t(9;22) BCR/ABL1/ASS1
Targeted Colorectal Tumor Mutation: Sequencing Panel
Targeted Gastric Tumor Mutation: Sequencing Panel
Targeted Lung Tumor Mutation: Sequencing Panel
Targeted Melanoma Mutation: Sequencing Panel
Targeted Ovarian Tumor Mutation: Sequencing Panel
Targeted Tumor Mutation: Sequencing Panel
TCF4 Gene Sequencing and Del/Dup
Telomere Length Measurement 6-Panel Test
Telomere Length Measurement 2-Panel Test
Tissue Culture Only
Trichorhinophalangeal Syndrome Type I Test
Trichorhinophalangeal Syndrome Type II Test
trisomy 12/12q13 (GLI)
Trisomy 8
 

U 

Uniparental Disomy Testing, General
Uveal Melanoma, Ocular Melanoma, Choroidal Melanoma
 

V 

Velocardiofacial Syndrome (FISH)
 

W 

Waardenburg Syndrome Type I Test
Waardenburg Syndrome Type III Test
Whole Chromosome Painting (FISH) (46 chromosomes)
Whole-Genome Chromosomal Microarray (CMA-ISCA) via aCGH and SNP
William's Syndrome
Williams Syndrome (FISH)
Williams Syndrome Test
Williams Syndrome, FISH Prenatal Diagnosis
Williams Syndrome, FISH Whole Blood
Williams-Beuren Region Duplication Syndrome Test
Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome Test
Wolf-Hirschhorn Syndrome (FISH)
Wolf-Hirschhorn Syndrome Test
Wolf-Hirschhorn Syndrome, FISH Prenatal Diagnosis
Wolf-Hirschhorn Syndrome, FISH Whole Blood
WT1-Related Disorders Test
 

X 

X and Y (Sex mismatch bone marrow transplant)
X-chromosome inactivation
X-inactivation (XIST)
X/Y Centromeres (Sex Determination)
 

Y 

Y Chromosome Detection Test