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Results: 41 to 60 of 83

Tests names and labsConditionsGenes, analytes, and microbesMethods

Skeletal diseases. NGS panel of 169 genes.

Genologica Medica
Spain
373169
  • C Sequence analysis of the entire coding region

Neuromuscular Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
13862
  • C Sequence analysis of the entire coding region

Myopathy, myofibrillar: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
109
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Myopathy NGS Panel

Fulgent Genetics
United States
18661
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Limb-Girdle Muscular Dystrophy

Asper Biogene Asper Biogene LLC
Estonia
8739
  • C Sequence analysis of the entire coding region

Muscle Polyneuropathies , Panel Massive Sequencing (NGS) 111 Genes

Reference Laboratory Genetics
Spain
159111
  • C Sequence analysis of the entire coding region

Myofibrillar Myopathy, Panel Massive Sequencing (NGS) 8 Genes

Reference Laboratory Genetics
Spain
98
  • C Sequence analysis of the entire coding region

Limb-Girdle Muscular Distrophy , Panel Massive Sequencing (NGS) 22 Genes

Reference Laboratory Genetics
Spain
2222
  • C Sequence analysis of the entire coding region

Autosomal Dominant Limb-Girdle Muscular Dystrophy, Panel Massive Sequencing (NGS) 3 Genes

Reference Laboratory Genetics
Spain
33
  • C Sequence analysis of the entire coding region

Congenital Myopathy and Distal Myopathy NGS panel

Asper Biogene Asper Biogene LLC
Estonia
7841
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MYOFIBRILLAR MYOPATHY

Laboratorio de Genetica Clinica SL
Spain
88
  • C Sequence analysis of the entire coding region

MUSCULAR DYSTROPHY, LIMB-GIRDLE TYPE 1A (AUT. DOMINANT) (MYOTILIN DEFICIENCY)

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

Neuromuscular Disorders NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
233144
  • C Sequence analysis of the entire coding region

Limb-Girdle Muscular Dystrophy Type 1A, Sequencing MYOT Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Muscular Dystrophy Advanced Evaluation

Athena Diagnostics Inc
United States
5333
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Limb Girdle Muscular Dystrophy Advanced Evaluation

Athena Diagnostics Inc
United States
2623
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Myofibrillar Myopathy Advanced Sequencing Evaluation

Athena Diagnostics Inc
United States
209
  • C Sequence analysis of the entire coding region

Distal Myopathy Advanced Sequencing Evaluation

Athena Diagnostics Inc
United States
2717
  • C Sequence analysis of the entire coding region

Myotilin-related myofibrillar myopathy without spheroid body

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

Results: 41 to 60 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.