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Results: 21 to 35 of 35

Tests names and labsConditionsGenes, analytes, and microbesMethods

BHLHA9 Single Gene

Fulgent Genetics
United States
311
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CKAP2L Single Gene

Fulgent Genetics
United States
331
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DDX59 Single Gene

Fulgent Genetics
United States
191
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DLL4 Single Gene

Fulgent Genetics
United States
461
  • 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

EOGT Single Gene

Fulgent Genetics
United States
461
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ERF Single Gene

Fulgent Genetics
United States
341
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FAT4 Single Gene

Fulgent Genetics
United States
911
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FBXW4 Single Gene

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ESCO2 Single Gene

Fulgent Genetics
United States
961
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS Panel

Fulgent Genetics
United States
543178
  • 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

Retinitis Pigmentosa NGS Panel

Fulgent Genetics
United States
329124
  • 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: 21 to 35 of 35

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.