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Results: 1 to 20 of 24

Tests names and labsConditionsGenes and analytesMethods

Deafness, non-syndromic sensorineural AR panel

Centogene AG - the Rare Disease Company
Germany
4443
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
123129
  • E Sequence analysis of select exons

Deafness, autosomal recessive type 29

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

Hereditary Hearing Loss and Deafness Sequencing Panel with CNV Detection

PreventionGenetics
United States
336195
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Audiome (hearing loss panel)

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
117106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Deafness, Autosomal Recessive 29 (DFNB29) via CLDN14 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
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hearing Loss NGS Panel

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

Nonsyndromic Hearing Loss NGS Panel

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

Hearing Loss Advanced Sequencing and CNV Evaluation

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

Hearing Loss: Deletion/Duplication Panel

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

Autosomal Recessive Hereditary Hearing Loss/Deafness , Panel Massive Sequencing (NGS) 39 Genes

Reference Laboratory Genetics
Spain
3839
  • C Sequence analysis of the entire coding region

Hearing Loss Sequencing Panel

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

DEAFNESS A.R. (39 genes)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
5139
  • C Sequence analysis of the entire coding region

DEAFNESS A.D. and A.R.

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

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

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

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

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

Non syndromic deafness AR and XL (NGS panel for 56 genes)

CGC Genetics
Portugal
5256
  • C Sequence analysis of the entire coding region

Deafness, autosomal recessive 29 (sequence analysis of CLDN14 gene)

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

CLDN14 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 24

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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