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Results: 21 to 40 of 77

Tests names and labsConditionsGenes, analytes, and microbesMethods

Usher Syndrome Type 1, Deafness, Autosomal Dominant 11 (DFNA11) and Deafness, Autosomal Recessive 2 (DFNB2) via the MYO7A Gene

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

Autosomal Dominant Hearing Loss. 25-gene NGS panel.

Genologica Medica
Spain
4823
  • C Sequence analysis of the entire coding region

Non-syndromic hearing loss panel. 95-gene NGS panel.

Genologica Medica
Spain
14694
  • C Sequence analysis of the entire coding region

Leber's congenital amaurosis panel. NGS panel of 26 genes.

Genologica Medica
Spain
4026
  • C Sequence analysis of the entire coding region

Retinal dystrophy panel. 260 gene NGS panel.

Genologica Medica
Spain
420257
  • C Sequence analysis of the entire coding region

Autosomal recessive hearing loss. 41-gene NGS panel.

Genologica Medica
Spain
6541
  • C Sequence analysis of the entire coding region

Mitochondrial genome sequencing

Molecular Vision Laboratory
United States
526339
  • C Sequence analysis of the entire coding region

Usher Syndrome (NGS Panel and Copy Number Analysis)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
1012
  • C Sequence analysis of the entire coding region

MYO7A

Institute for Human Genetics University Medical Center Freiburg
Germany
31
  • C Sequence analysis of the entire coding region

Síndrome de Usher (WES based NGS panel of 13 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
2413
  • C Sequence analysis of the entire coding region

Retinitis pigmentosa (WES based NGS panel of 189 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
286189
  • C Sequence analysis of the entire coding region

Diseases of the posterior ocular segment (WES based NGS panel of 307 gene, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
493306
  • C Sequence analysis of the entire coding region

Ciliopathies (WES based NGS panel of 202 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
245201
  • C Sequence analysis of the entire coding region

Deafness, autosomal recessive 18A (sequence analysis of USH1C gene)

Unilabs Genetics CGC Genetics
Portugal
31
  • C Sequence analysis of the entire coding region

Usher syndrome type 1B (deletion/duplication analysis on MYO7A gene)

Unilabs Genetics CGC Genetics
Portugal
31
  • D Deletion/duplication analysis

MYO7A Prenatal Sequence Analysis (GeneAware) (Prenatal Sequence Analysis)

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

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

Hearing Loss, Comprehensive Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
14284
  • C Sequence analysis of the entire coding region

Syndromic Hearing Loss NGS Panel

Fulgent Genetics
United States
22383
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hearing Loss NGS Panel

Fulgent Genetics
United States
332167
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 77

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.