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Results: 41 to 55 of 55

Tests names and labsConditionsGenes, analytes, and microbesMethods

USHER syndrome panel

Molecular Vision Laboratory
United States
2414
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel

Molecular Vision Laboratory
United States
372283
  • C Sequence analysis of the entire coding region

MYO7A Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • D Deletion/duplication analysis

MYO7A Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sensorineural Hearing Loss

Asper Biogene Asper Biogene LLC
Estonia
8379
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Usher Syndrome NGS Panel

Fulgent Genetics
United States
2112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Deafness, autosomal recessive 2

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ciliopathies NGS Panel

Fulgent Genetics
United States
14197
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Deafness, autosomal recessive 2

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Usher Syndrome Panel by next-generation sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
189
  • C Sequence analysis of the entire coding region

Hereditary Hearing Loss-Common and Non-Syndromic Hearing Loss Panel

Genome Diagnostics Laboratory Hospital For Sick Children
Canada
6457
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

OtoSeq Hearing Loss Panel by next-generation sequencing (NGS)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
3623
  • C Sequence analysis of the entire coding region

MYO7A Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 41 to 55 of 55

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.