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Results: 61 to 73 of 73

Tests names and labsConditionsGenes, analytes, and microbesMethods

Cardio-channelopathy-gene-panel

MVZ Dr. Eberhard & Partner Dortmund
Germany
3533
  • C Sequence analysis of the entire coding region

Brugada Syndrome 3

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

CACNA1C 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

Invitae Brugada Syndrome Panel

Invitae
United States
78
  • D Deletion/duplication analysis
  • 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

Short QT Syndrome NGS Panel

Fulgent Genetics
United States
166
  • 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

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism NGS Panel

Fulgent Genetics
United States
170106
  • 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

Comprehensive Arrhythmia NGS Panel

Fulgent Genetics
United States
18476
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Brugada Syndrome type 3

John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
United States
11
  • C Sequence analysis of the entire coding region

Results: 61 to 73 of 73

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.