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Results: 21 to 40 of 64

Tests names and labsConditionsGenes, analytes, and microbesMethods

CardioNext®

Ambry Genetics
United States
18992
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia Exome

Genetic Services Laboratory University of Chicago
United States
289481
  • C Sequence analysis of the entire coding region

FXN Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
11
  • T Targeted variant analysis

FXN Sequence Analysis

Baylor Genetics
United States
11
  • C Sequence analysis of the entire coding region

Friedreich Ataxia Repeat Expansion Analysis

Baylor Genetics
United States
11
  • T Targeted variant analysis

Ataxia panel. NGS panel of 157 genes.

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

Spastic paraplegia panel

Genologica Medica
Spain
10060
  • C Sequence analysis of the entire coding region

Friedreich Ataxia Mutation Analyis

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • T Targeted variant analysis

Friedreich Ataxia

Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center
Turkey
11
  • C Sequence analysis of the entire coding region

Friedreich Ataxia Genetic Testing (Repeat Expansion)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
11
  • E Sequence analysis of select exons

Comprehensive Ataxia Repeat Expansion Panel (SCA 1, 2, 3, 6, 7, 8, 10, 12, 17, 36, DRPLA & FRDA)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
1212
  • T Targeted variant analysis

Early-Onset Ataxia NGS Panel

Fulgent Genetics
United States
505132
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy NGS Panel

Fulgent Genetics
United States
450128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Oxidative Phosphorylation Disorders NGS Panel

Fulgent Genetics
United States
416235
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Late-Onset Ataxia NGS Panel

Fulgent Genetics
United States
13356
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia NGS Panel

Fulgent Genetics
United States
533149
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia Repeat Expansion Analysis

Fulgent Genetics
United States
1915
  • T Targeted variant analysis

FXN (Freidrich's Ataxia) Repeat Expansion

Fulgent Genetics
United States
11
  • T Targeted variant analysis

Friedreich`s ataxia

Genetics Service Unit BRIC-National Institute of Biomedical Genomics
India
11
  • T Targeted variant analysis

Friedreich ataxia

Molecular Genetics Laboratory North York General Hospital
Canada
11
  • T Targeted variant analysis

Results: 21 to 40 of 64

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.