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Results: 21 to 33 of 33

Tests names and labsConditionsGenes, analytes, and microbesMethods

LZTR1 Single Gene

Fulgent Genetics
United States
571
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MEGF8 Single Gene

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

NRAS Single Gene

Fulgent Genetics
United States
1781
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DVL1 Single Gene

Fulgent Genetics
United States
701
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NALCN Single Gene

Fulgent Genetics
United States
511
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Full Comprehensive Cancer Panel

Fulgent Genetics
United States
329127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nervous System / Brain Cancer Comprehensive Panel

Fulgent Genetics
United States
13327
  • 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

Clinical Exome

Fulgent Genetics
United States
51294672
  • 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

Connective Tissue NGS Panel

Fulgent Genetics
United States
18760
  • 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

Marfan Syndrome and Thoracic Aortic Aneurysm and Dissection NGS Panel

Fulgent Genetics
United States
6531
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 33 of 33

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.