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Results: 61 to 70 of 70

Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • 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

Spinocerebellar Ataxia Panel (SCA1, SCA2, SCA3, SCA6, SCA7)

Molecular Genetics Laboratory BC Children's and BC Women's Hospitals
Canada
55
  • T Targeted variant analysis

Comprehensive Eye Disorders NGS Panel

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

Spinocerebellar ataxia 7

Center for Human Genetics, Inc
United States
11
  • T Targeted variant analysis

Spinocerebellar Ataxia 07

Praxis fuer Humangenetik Wien
Austria
11
  • T Targeted variant analysis

Spinocerebellar Ataxia Type 7

MGZ Medical Genetics Center
Germany
11
  • T Targeted variant analysis

SCA 7

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
11
  • T Targeted variant analysis

Spinocerebellar Ataxia: Panel of SCA1, SCA2, SCA3, SCA6, SCA7

Defense Health Agency Genetics Reference Laboratory United States Air Force
United States
55
  • T Targeted variant analysis

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.