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Results: 1 to 19 of 19

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

Knuckle pads and leukonychia sensorineural deafness

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GJB2 Sequence Analysis (Prenatal Diagnosis)

Baylor Miraca Genetics Laboratories
United States
71
  • T Targeted variant analysis

GJB2 Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Miraca Genetics Laboratories
United States
71
  • T Targeted variant analysis

GJB2 Sequence Analysis

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

GJB2 Deletion/Duplication Analysis (Prenatal Diagnosis)

Baylor Miraca Genetics Laboratories
United States
71
  • D Deletion/duplication analysis

GJB2 Deletion/Duplication Analysis

Baylor Miraca Genetics Laboratories
United States
71
  • D Deletion/duplication analysis

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

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

Connexin 26, Full Gene Sequencing

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

Single gene testing GJB2

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

USHER syndrome panel

Molecular Vision Laboratory
United States
3115
  • 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 Clinical Diagnostics Lab Fulgent Diagnostics
United States
81
  • 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
United States
15992
  • C Sequence analysis of the entire coding region

Hearing Loss NGS Panel

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

DEAFNESS, AUTOSOMAL RECESSIVE 1A; DFNB1A

Human Genetics Ruhr University
Germany
101
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Hearing Loss, Nonsyndromic Panel (GJB2) Sequencing, (GJB6) 2 Deletions and Mitochondrial DNA 2 Mutations

ARUP Laboratories, Molecular Genetics University of Utah ARUP Lab
United States
94
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 19 of 19

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.