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Results: 41 to 48 of 48

Tests names and labsConditionsGenes, analytes, and microbesMethods

CSRP3 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

Clinical Exome

Fulgent Genetics
United States
51284672
  • 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

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

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • 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

Results: 41 to 48 of 48

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.