U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

Results: 21 to 40 of 66

Tests names and labsConditionsGenes, analytes, and microbesMethods

Limb Girdle Muscular Dystrophy Type 2Y via the TOR1AIP1 Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Comprehensive Muscular Dystrophy Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
11452
  • D Deletion/duplication analysis

Invitae Limb-Girdle Muscular Dystrophy Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
9137
  • D Deletion/duplication analysis

Invitae Comprehensive Neuromuscular Disorders Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
353208
  • D Deletion/duplication analysis

Limb Girdle Muscular Dystrophy (LGMD) Panel

PreventionGenetics, part of Exact Sciences
United States
3435
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GeneSeq® Neuro: Limb-Girdle and Emery-Dreifuss Muscular Dystrophies

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
243
  • C Sequence analysis of the entire coding region

Neuromuscular Disorders Panel

Baylor Genetics
United States
1142
  • C Sequence analysis of the entire coding region

Neuromuscular diseases panel_v.2.0

CGC Genetics Unilabs
Portugal
17248
  • C Sequence analysis of the entire coding region

Cardiovascular panel _v.2.0

CGC Genetics Unilabs
Portugal
1264
  • C Sequence analysis of the entire coding region

Cardiomyopathy panel_v.2.0

CGC Genetics Unilabs
Portugal
1203
  • C Sequence analysis of the entire coding region

Neuromuscular Diseases Panel (Expanded)

Mendelics
Brazil
1288
  • C Sequence analysis of the entire coding region

Neuromuscular Diseases Panel (DNAmplo)

Mendelics
Brazil
1109
  • C Sequence analysis of the entire coding region

Arrhythmia Panel

Mendelics
Brazil
1311
  • C Sequence analysis of the entire coding region

Cardiomyopathy Panel

Mendelics
Brazil
1311
  • C Sequence analysis of the entire coding region

HEREDITARY ATAXIAS EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
11202
  • E Sequence analysis of select exons

DYSTONIA EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1119
  • E Sequence analysis of select exons

LIMB-GIRDLE MUSCULAR DYSTROPHY EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
154
  • E Sequence analysis of select exons

MUSCULAR DISORDERS- EMCG GLOBAL EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1416
  • E Sequence analysis of select exons

MUSCULAR DYSTROPHIES/ MYOPATHIES PANEL

Laboratorio de Genetica Clinica SL
Spain
1250
  • E Sequence analysis of select exons

HYPERTROPHIC CARDIOMYOPATHY EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1197
  • E Sequence analysis of select exons

Results: 21 to 40 of 66

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.