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Results: 1 to 20 of 51 (representing 30 labs)

Tests names and labsConditionsGenes and analytesMethods

Spinocerebellar Ataxia Panel (SCA1,2,3,6, and 7)

Center for Genetics at Saint Francis Saint Francis Hospital
United States
55
  • T Targeted variant analysis

Spinocerebellar ataxia type 2

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ATXN2. CAG expansion detection by PCR

Instituto de Medicina Genomica
Spain
11
  • T Targeted variant analysis

ATXN1, ATXN2, ATXN3, ATXN7, CACNA1A. Detection of the expansions associated to SCA1, SCA2, SCA3, SCA6 and SCA7 by PCR

Instituto de Medicina Genomica
Spain
65
  • T Targeted variant analysis

SCA Panel (SCA1, 2, 3, 6, 7) test

Neurogenetics Department Cyprus Institute of Neurology and Genetics
Cyprus
55
  • T Targeted variant analysis

Ataxin 2 (ATXN2) gene CAG triplet repeat test

Neurogenetics Department Cyprus Institute of Neurology and Genetics
Cyprus
11
  • T Targeted variant analysis

Spinocerebellar ataxia type 2

Molecular Diagnostic Laboratory Diagnostic Services of Manitoba, Health Sciences Centre site
Canada
11
  • T Targeted variant analysis

Spinocerebellar ataxia panel

LifeLabs Genetics
Canada
2925
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ataxia, Complete Dominant Evaluation

Athena Diagnostics Inc
United States
3125
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ataxia, Comprehensive Evaluation

Athena Diagnostics Inc
United States
4442
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ataxia, Common Repeat Expansion Evaluation

Athena Diagnostics Inc
United States
88
  • T Targeted variant analysis

Single gene testing ATXN2

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Spinocerebellar ataxia

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
4337
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Exome

DNA CONSULT GENETICA E BIOTECNOLOGIA LTDA.
Brazil
5968
  • T Targeted variant analysis

Spinocerebellar Ataxia

GeneTech ATS GeneTech Private Limited
India
11
  • T Targeted variant analysis

Spinocerebellar ataxia type 2

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Spinocerebellar Ataxia 2

Molecular Diagnostics Division Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

Atypical Parkinson syndrome Panel

CeGaT GmbH
Germany
2524
  • C Sequence analysis of the entire coding region

Ataxia and differential diagnoses Panel

CeGaT GmbH
Germany
174204
  • C Sequence analysis of the entire coding region

Choreatic Movement Disorders Panel

CeGaT GmbH
Germany
1622
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 51

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.

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