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Results: 21 to 40 of 83

Tests names and labsConditionsGenes, analytes, and microbesMethods

Ataxia Repeat Expansion Panel

Genetic Services Laboratory University of Chicago
United States
1313
  • X Mutation scanning of select exons

Invitae Epilepsy Panel

Invitae
United States
466297
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Next Generation Sequencing for FHM, EA1, EA2, SCA6, CADASIL, CARASIL, COL4A1/2, Fabry Disease, Small Vessel Disease, Epilepsy

Genomics Research Centre Diagnostics Clinic Queensland Unstitute of Technology
Australia
1812
  • C Sequence analysis of the entire coding region

Early Infantile Epileptic Encephalopathy Panel

PreventionGenetics, part of Exact Sciences
United States
144124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Spinocerebellar ataxia type 6

Molecular Diagnostic Laboratory Diagnostic Services, Shared Health Manitoba
Canada
11
  • T Targeted variant analysis

CACNA1A

Institute for Human Genetics University Medical Center Freiburg
Germany
41
  • C Sequence analysis of the entire coding region

Spinocerebellar ataxia 6 (SCA6, CAG expansion on CACNA1A gene)

CGC Genetics Unilabs
Portugal
11
  • T Targeted variant analysis

Genetic Test for Spinocerebellar Ataxias - SCA1, SCA2, SCA3, SCA6, SCA7, SCA17 and DRPLA

CGPP - Center for Predictive and Preventive Genetics IBMC - Institute for Cell and Molecular Biology
Portugal
77
  • D Deletion/duplication analysis

Genetic Test for Spinocerebellar Ataxia Type 6 - SCA6

CGPP - Center for Predictive and Preventive Genetics IBMC - Institute for Cell and Molecular Biology
Portugal
11
  • D Deletion/duplication analysis

Hereditary ataxias. NGS panel of 139 genes.

Genologica Medica
Spain
220139
  • C Sequence analysis of the entire coding region

Ataxia panel. NGS panel of 157 genes.

Genologica Medica
Spain
247156
  • C Sequence analysis of the entire coding region

Epileptic encephalopathy panel. 128-gene NGS panel.

Genologica Medica
Spain
197128
  • C Sequence analysis of the entire coding region

Migraine panel. NGS panel of 10 genes.

Genologica Medica
Spain
3010
  • C Sequence analysis of the entire coding region

Complete epilepsy panel. NGS panel of 283 genes.

Genologica Medica
Spain
409283
  • C Sequence analysis of the entire coding region

SCA Panel (Type 1,2,3,6,7)

Duzen Laboratories Duzen BBAGUAS
Turkey
45
  • T Targeted variant analysis

Spinocerebellar Ataxia (SCA) Type 6

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

Spinocerebellar Ataxia Type 6 Repeat Analysis

GeneDx
United States
11
  • T Targeted variant analysis

Spinocerebellar Ataxia Repeat Expansion Analysis

GeneDx
United States
66
  • T Targeted variant analysis

Spinocerebellar Ataxia Expansion Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
55
  • E Sequence analysis of select exons

Spinocerebellar Ataxia Type 6 Expansion Analysis

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
11
  • E Sequence analysis of select exons

Results: 21 to 40 of 83

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.