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Results: 41 to 60 of 148

Tests names and labsConditionsGenes, analytes, and microbesMethods

GJB2 Sequencing, Full Gene

Molecular Diagnostic Laboratory LabCorp
United States
11
  • C Sequence analysis of the entire coding region

GJB2 Sequencing, Family-targeted (Single Exon Sequencing - Known Mutation)

Molecular Diagnostic Laboratory LabCorp
United States
11
  • E Sequence analysis of select exons

Deafness, Autosomal Dominant 3B (DFNA3B) and Deafness, Autosomal Recessive 1B (DFNB1B) via the GJB6 Gene

PreventionGenetics, part of Exact Sciences
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GJB6 Deletion Analysis

Baylor Genetics
United States
41
  • T Targeted variant analysis

GJB2 Sequence Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
71
  • T Targeted variant analysis

GJB2 Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
71
  • T Targeted variant analysis

GJB2 Sequence Analysis

Baylor Genetics
United States
71
  • C Sequence analysis of the entire coding region

GJB2 Deletion/Duplication Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
71
  • D Deletion/duplication analysis

GJB2 Deletion/Duplication Analysis

Baylor Genetics
United States
71
  • D Deletion/duplication analysis

Connexin Test (GJB2 Sequencing and DFNB1 (GJB6) Deletions)

Laboratory for Molecular Medicine Mass General Brigham Personalized Medicine
United States
62
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Deafness, Autosomal Dominant 3A (DFNA3A) and Deafness, Autosomal Recessive 1A (DFNB1A) via the GJB2 Gene

PreventionGenetics, part of Exact Sciences
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Connexin Hearing Loss Panel

Center for Genetics at Saint Francis Saint Francis Hospital
United States
22
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Hearing Loss

Molecular Diagnostic Laboratory Diagnostic Services, Shared Health Manitoba
Canada
12
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GJB2 MLPA

Institute for Human Genetics University Medical Center Freiburg
Germany
71
  • D Deletion/duplication analysis

GJB3 MLPA

Institute for Human Genetics University Medical Center Freiburg
Germany
31
  • D Deletion/duplication analysis

GJB6 MLPA

Institute for Human Genetics University Medical Center Freiburg
Germany
41
  • D Deletion/duplication analysis

DEAFNESS, AUTOSOMAL RECESSIVE 1A

BioReference Health
United States
11
  • T Targeted variant analysis

Connexin 26 (GJB2) Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
11
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia panel. 23-gene NGS panel.

Genologica Medica
Spain
6023
  • C Sequence analysis of the entire coding region

Autosomal Dominant Hearing Loss. 25-gene NGS panel.

Genologica Medica
Spain
4823
  • C Sequence analysis of the entire coding region

Results: 41 to 60 of 148

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.