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Results: 41 to 60 of 64

Tests names and labsConditionsGenes, analytes, and microbesMethods

ATAXIA, FRIEDREICH (FRDA)

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ataxia, Comprehensive Evaluation

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

Ataxia, Complete Recessive Evaluation

Athena Diagnostics
United States
2118
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Single gene testing FXN

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

Friedreich's ataxia mutation analysis

Diagnostics Division CENTRE FOR DNA FINGERPRINTING AND DIAGNOSTICS
India
31
  • T Targeted variant analysis

FXN

Institute of Human Genetics Medical University Innsbruck
Austria
11
  • S Mutation scanning of the entire coding region

Friedreich Ataxie, FXN

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • D Deletion/duplication analysis

Friedreich Ataxie, FXN

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • E Sequence analysis of select exons

Friedreich Ataxie, FXN

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

FXN Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy NGS Panel

Fulgent Genetics
United States
37586
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia, Friedreich (FXN) Evaluation

Athena Diagnostics
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Friedreich Ataxia (FXN) DNA Sequencing Test

Athena Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

Friedreich Ataxia DNA Test

Athena Diagnostics
United States
11
  • T Targeted variant analysis

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

Friedreich Ataxia

Molecular Genetics Laboratory BC Children's and BC Women's Hospitals
Canada
11
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 60 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.