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Results: 1 to 20 of 24

Tests names and labsConditionsGenes and analytesMethods

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
123129
  • -- Sequence analysis of select exons

Deafness, autosomal dominant type 4

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis

Hereditary Hearing Loss and Deafness Sequencing Panel with CNV Detection

PreventionGenetics
United States
337195
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Deafness, Autosomal Dominant 4A (DFNA4A) via MYH14 Gene Sequencing with CNV Detection

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

OtoSCOPE

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
181153
  • -- Deletion/duplication analysis
  • -- Sequence analysis of the entire coding region

Deafness, autosomal dominant: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
4039
  • C Sequence analysis of the entire coding region

Comprehensive Hearing Loss NGS Panel

Fulgent Genetics
United States
333167
  • -- Deletion/duplication analysis
  • -- Sequence analysis of the entire coding region

Nonsyndromic Hearing Loss NGS Panel

Fulgent Genetics
United States
14799
  • -- Deletion/duplication analysis
  • -- Sequence analysis of the entire coding region

Hearing Loss Advanced Sequencing and CNV Evaluation

Athena Diagnostics Inc
United States
249184
  • -- Deletion/duplication analysis
  • -- Sequence analysis of the entire coding region

Hearing Loss: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
15491
  • -- Deletion/duplication analysis

Autosomal Dominant Hereditary Hearing Loss/Deafness , Panel Massive Sequencing (NGS) 31 Genes

Reference Laboratory Genetics
Spain
3131
  • C Sequence analysis of the entire coding region

Hearing Loss Sequencing Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
10891
  • -- Sequence analysis of the entire coding region

DEAFNESS A.D. and A.R.

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
6557
  • -- Sequence analysis of the entire coding region

DEAFNESS A.D.

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2426
  • C Sequence analysis of the entire coding region

Non syndromic deafness AD, AR and XL (NGS panel for 79 genes)

CGC Genetics
Portugal
7479
  • -- Sequence analysis of the entire coding region

Syndromic and non syndromic deafness (NGS panel for 127 genes)

CGC Genetics
Portugal
118127
  • -- Sequence analysis of the entire coding region

Non syndromic deafness AD (NGS panel for 33 genes)

CGC Genetics
Portugal
3032
  • C Sequence analysis of the entire coding region

Deafness, autosomal dominant 4 (sequence analysis of MYH14 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

MYH14

MGZ Medical Genetics Center
Germany
21
  • C Sequence analysis of the entire coding region

MYH14 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 24

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