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Results: 1 to 20 of 25 (representing 13 labs)

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Baby Genes Targeted Panel

Baby Genes Inc.
United States
8990
  • 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 26, Full Gene Sequencing

ARUP Laboratories, Molecular Genetics and Genomics
United States
61
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GJB2 single gene sequencing

Molecular Vision Laboratory
United States
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Common Hearing Loss Panel

Molecular Vision Laboratory
United States
143
  • C Sequence analysis of the entire coding region

Single gene testing GJB2

CeGaT GmbH
Germany
71
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel

Molecular Vision Laboratory
United States
372287
  • C Sequence analysis of the entire coding region

Ichthyoses and related disorders of cornification Panel

CeGaT GmbH
Germany
4265
  • C Sequence analysis of the entire coding region

GJB2

Division Human Genetics Medical University Innsbruck
Austria
71
  • S Mutation scanning of the entire coding region

GJB2

Fulgent Genetics
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Expanded Hearing Loss Panel, Sequencing (56 Genes) and Deletion/Duplication (53 Genes)

ARUP Laboratories, Molecular Genetics and Genomics
United States
1756
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GJB2

Institute for Human Genetics University Clinic Freiburg
Germany
71
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hearing Loss: Sequencing Panel

Emory Genetics Laboratory Emory University School of Medicine
United States
15992
  • C Sequence analysis of the entire coding region

Hearing Loss NGS Panel

Fulgent Genetics
United States
202103
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 25

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.

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