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Results: 61 to 70 of 70

Tests names and labsConditionsGenes, analytes, and microbesMethods

Autosomal Dominant Retinitis Pigmentosa

Asper Biogene Asper Biogene LLC
Estonia
2526
  • D Deletion/duplication analysis
  • 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

Ataxia (AD/AR) panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
2316
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Retinitis Pigmentosa NGS Panel

Fulgent Genetics
United States
329124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Spinocerebellar Ataxia 14

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

Spinocerebellar Ataxia 14

MedGene
Slovakia
11
  • E Sequence analysis of select exons

Comprehensive Eye Disorders NGS Panel

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

Spinocerebellar Ataxia 14

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

Spinocerebellar Ataxia 14

Praxis fuer Humangenetik Wien
Austria
11
  • E Sequence analysis of select exons

Results: 61 to 70 of 70

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.