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Results: 61 to 72 of 72

Tests names and labsConditionsGenes, analytes, and microbesMethods

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dihydropyrimidine Dehydrogenase (DPYD), 3 Variants

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
21
  • T Targeted variant analysis

Pharmacogenetic panel

Diagnosticum Center for Human Genetics
Germany
4629
  • T Targeted variant analysis

Familial pyrimidinemia

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

DPYD

Institute of Human Genetics Medical University Innsbruck
Austria
11
  • S Mutation scanning of the entire coding region

DPYD Single Gene

Fulgent Genetics
United States
11
  • 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

Lysosomal Disorders NGS Panel

Fulgent Genetics
United States
186106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Organic Acids, Comprehensive, Quantitative, Urine

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
3857
  • A Analyte

Dihydropyrimidin Dehydrogenase deficiency

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Dihydropyrimidine dehydrogenase Deficiency (DPYD)

Amsterdam UMC, Location AMC Laboratory Genetic Metabolic Diseases, LGMD
Netherlands
11
  • A Analyte
  • E Enzyme assay
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 61 to 72 of 72

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.