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Results: 1 to 20 of 20

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Glomerular Proteinuria NGS Panel

Fulgent Genetics
United States
18276
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Microcephaly-Capillary Malformation Syndrome (STAMBP Single Gene Test)

Fulgent Genetics
United States
321
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Early-Onset Ataxia NGS Panel

Fulgent Genetics
United States
505132
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypomagnesemia NGS Panel

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

Leigh Disease NGS Panel

Fulgent Genetics
United States
16375
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Oxidative Phosphorylation Disorders NGS Panel

Fulgent Genetics
United States
416235
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ataxia NGS Panel

Fulgent Genetics
United States
533149
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

STAMBP Single Gene

Fulgent Genetics
United States
321
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

WDR73 Single Gene

Fulgent Genetics
United States
661
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

POC1A Single Gene

Fulgent Genetics
United States
371
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CRIPT Single Gene

Fulgent Genetics
United States
221
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PAM16 Single Gene

Fulgent Genetics
United States
291
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FBXL4 Single Gene

Fulgent Genetics
United States
431
  • 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

mtDNA Depletion Syndrome NGS Panel

Fulgent Genetics
United States
8616
  • 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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • 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

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 20

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.