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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hypomagnesemia NGS Panel

Fulgent Genetics
United States
12123
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TMEM98 Single Gene

Fulgent Genetics
United States
101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PIGT Single Gene

Fulgent Genetics
United States
431
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHMP1A Single Gene

Fulgent Genetics
United States
251
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHAMP1 Single Gene

Fulgent Genetics
United States
231
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CTCF Single Gene

Fulgent Genetics
United States
141
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DMBX1 Single Gene

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PCYT1A Single Gene

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

PDGFRB Single Gene

Fulgent Genetics
United States
811
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FAM111A Single Gene

Fulgent Genetics
United States
901
  • 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

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • 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 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.