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Results: 21 to 27 of 27

Tests names and labsConditionsGenes, analytes, and microbesMethods

TMC1 Single Gene

Fulgent Genetics
United States
21
  • 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
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TMC1 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
21
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Usher Syndrome

Asper Biogene Asper Biogene LLC
Estonia
1920
  • D Deletion/duplication analysis
  • 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

Results: 21 to 27 of 27

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.