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Results: 1 to 8 of 8

Tests names and labsConditionsGenes, analytes, and microbesMethods

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

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

GJB2 Prenatal Sequence Analysis (GeneAware) (Prenatal Sequence Analysis)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

Super Panel Plus

NxGen MDx
United States
116117
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Super Panel 113

NxGen MDx
United States
113115
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hearing Loss Test

GeneDx
United States
56150
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Mutation analysis of Connexin 26 gene and testing of common deletions in Connexin 30 gene

Diagnostics Division CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS
India
42
  • E Sequence analysis of select exons

Sensorineural Hearing Loss

Asper Biogene Asper Biogene LLC
Estonia
8379
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Non-syndromic Hearing Loss

GeneTech ATS GeneTech Private Limited
India
12
  • E Sequence analysis of select exons

Results: 1 to 8 of 8

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.