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Results: 1 to 12 of 12

Tests names and labsConditionsGenes, analytes, and microbesMethods

SETD5 Single Gene

Fulgent Genetics
United States
181
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ZBTB20 Single Gene

Fulgent Genetics
United States
641
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KCNH1 Single Gene

Fulgent Genetics
United States
751
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KMT2A Single Gene

Fulgent Genetics
United States
371
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ATP6V1B2 Single Gene

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

PACS1 Single Gene

Fulgent Genetics
United States
221
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GPR101 Single Gene

Fulgent Genetics
United States
481
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Renal / Urinary Cancer Comprehensive Panel

Fulgent Genetics
United States
54327
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sarcoma Comprehensive Panel

Fulgent Genetics
United States
64526
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Full Comprehensive Cancer Panel

Fulgent Genetics
United States
1166141
  • 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

Intellectual Disability NGS Panel

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

Results: 1 to 12 of 12

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.