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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

Pachyonychia Congenita NGS Panel

Fulgent Genetics
United States
228
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Full Focus Cancer Panel

Fulgent Genetics
United States
8230
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

AAGAB Single Gene

Fulgent Genetics
United States
91
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RPS20 Single Gene

Fulgent Genetics
United States
201
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LRRFIP2 Single Gene

Fulgent Genetics
United States
211
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BUB1 Single Gene

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

COL14A1 Single Gene

Fulgent Genetics
United States
71
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GREM1 Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Colorectal Cancer Comprehensive Panel

Fulgent Genetics
United States
7722
  • 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

Colorectal Cancer Focus Panel

Fulgent Genetics
United States
6218
  • 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
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 13 of 13

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.