U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

See more countries

Results: 181 to 200 of 200

Tests names and labsConditionsGenes, analytes, and microbesMethods

SGCD Single Gene

Fulgent Genetics
United States
21
  • 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

Dilated Cardiomyopathy NGS Panel

Fulgent Genetics
United States
18278
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Limb-Girdle Muscular Dystrophy NGS Panel

Fulgent Genetics
United States
5120
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SGCD

MGZ Medical Genetics Center
Germany
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular Dystrophy: Limb Girdle - autosomal recessive

MGZ Medical Genetics Center
Germany
716
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sudden Death Syndrome NGS Panel

Fulgent Genetics
United States
16868
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuromuscular NGS Panel

Fulgent Genetics
United States
259112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
12861
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Muscular dystrophy, limb-girdle 2F

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy, dilated, 1L

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiovascular NGS Panel

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

Muscular Dystrophies NGS Panel

Fulgent Genetics
United States
12542
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Muscular dystrophy, limb-girdle 2F

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiomyopathy, dilated, 1L

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
13098
  • C Sequence analysis of the entire coding region

Dilated Cardiomyopathy Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
10073
  • C Sequence analysis of the entire coding region

Cardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center, Location AMC
Netherlands
551
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Limb-Girdle Muscular Dystrophy type 2 (LGMD2)

Laboratory of Human Genetics GENOMED Health Care Center
Poland
113
  • C Sequence analysis of the entire coding region

Results: 181 to 200 of 200

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.