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Results: 1 to 11 of 11

Tests names and labsConditionsGenes, analytes, and microbesMethods

Micromelic Dysplasia NGS Panel

Fulgent Genetics
United States
14024
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Retinopathy and Optic Atrophy NGS Panel

Fulgent Genetics
United States
563241
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Robinow Syndrome NGS Panel

Fulgent Genetics
United States
765
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Coffin-Siris Syndrome NGS Panel

Fulgent Genetics
United States
8211
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SMCHD1 Single Gene

Fulgent Genetics
United States
151
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SOX11 Single Gene

Fulgent Genetics
United States
691
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TUBGCP4 Single Gene

Fulgent Genetics
United States
241
  • 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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Microcephaly NGS Panel

Fulgent Genetics
United States
32275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 11 of 11

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.