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Results: 1 to 20 of 21

Tests names and labsConditionsGenes, analytes, and microbesMethods

Muscular Dystrophy Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
175
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Genomic Unity Neuromuscular Disorders Analysis (includes STR analysis of CNBP, DMPK, GIPC1, LRP12, RFC1 and VWA1 genes).

Variantyx, Inc.
United States
53
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Genomic Unity Muscular Dystrophy Analysis

Variantyx, Inc.
United States
451
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophy, Myopathy and Myasthenia Panel

Mendelics
Brazil
391
  • C Sequence analysis of the entire coding region

Inclusion Body Myopathy NGS Panel

Fulgent Genetics
United States
215
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuronal Migration Disorders NGS Panel

Fulgent Genetics
United States
39283
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cerebral Cortical Malformation NGS Panel

Fulgent Genetics
United States
21042
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2S

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

Comprehensive Muscular Dystrophy / Myopathy Panel

Blueprint Genetics
Finland
273
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TNPO3 Single Gene

Fulgent Genetics
United States
161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

POMK Single Gene

Fulgent Genetics
United States
561
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HNRNPA2B1 Single Gene

Fulgent Genetics
United States
101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HNRNPA1 Single Gene

Fulgent Genetics
United States
131
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

B4GAT1 Single Gene

Fulgent Genetics
United States
451
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GMPPB Single Gene

Fulgent Genetics
United States
491
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Myasthenic Syndrome NGS Panel

Fulgent Genetics
United States
10528
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dystroglycan-Related Congenital Muscular Dystrophy NGS Panel

Fulgent Genetics
United States
6713
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuromuscular NGS Panel

Fulgent Genetics
United States
280112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis NGS Panel

Fulgent Genetics
United States
8443
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 21

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.