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Results: 1 to 9 of 9

Tests names and labsConditionsGenes, analytes, and microbesMethods

RNF216 Single Gene

Fulgent Genetics
United States
301
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SPRY4 Single Gene

Fulgent Genetics
United States
381
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HS6ST1 Single Gene

Fulgent Genetics
United States
411
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

IL17RD Single Gene

Fulgent Genetics
United States
441
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DUSP6 Single Gene

Fulgent Genetics
United States
401
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FGF17 Single Gene

Fulgent Genetics
United States
401
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FEZF1 Single Gene

Fulgent Genetics
United States
411
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FLRT3 Single Gene

Fulgent Genetics
United States
391
  • 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

Results: 1 to 9 of 9

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.