DCLRE1B

OMIMHGNC

Synonym(s): SNM1B, FLJ12810, FLJ13998

Locus: 1p13.2

Tests

Test Type
Molecular (2)
Multi-Gene Panel (1)
Multi-Method Panel (1)
Test Method
Del/Dup (CNV) (1)
Sequencing, Capillary (Sanger) (1)
Sequencing, Next Gen (2)
Lab Location
USA(1)
Portugal(1)
 
TAT: 4-5 Weeks
price: contact lab
DCLRE1B
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
CID with associated or syndromic features - Inherited bone marrow failure/dyskeratosis congenital (NGS panel of 10 genes)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal