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Results: 21 to 37 of 37

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Thrombosis, Platelet Disorder, and Coagulation Deficiency NGS Panel

Fulgent Genetics
United States
14682
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bernard-Soulier Syndrome NGS Panel

Fulgent Genetics
United States
43
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Plus Panel

Fulgent Genetics
United States
716335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Panel

Fulgent Genetics
United States
636298
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Plus Panel

Fulgent Genetics
United States
661306
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Platelet Function Related Disorders , Panel Massive Sequencing (NGS) 17 Genes

Reference Laboratory Genetics
Spain
1517
  • C Sequence analysis of the entire coding region

Thrombocytopenia and Related Disorders , Panel Massive Sequencing (NGS) 14 Genes

Reference Laboratory Genetics
Spain
1415
  • C Sequence analysis of the entire coding region

Bleeding Disorders , Panel Massive Sequencing (NGS) 23 Genes

Reference Laboratory Genetics
Spain
2222
  • C Sequence analysis of the entire coding region

VWD Platelet-Type Sequence Analysis

Versiti Diagnostic Laboratories Versiti, Inc
United States
21
  • C Sequence analysis of the entire coding region

GP1BA Single Gene

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

Coagulation Deficiency NGS Panel

Fulgent Genetics
United States
5624
  • 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

Thrombocytopenia NGS Panel

Fulgent Genetics
United States
3215
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

von Willebrand disease, platelet-type

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

von Willebrand disease, platelet-type

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Pseudo von Willebrand disease

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Results: 21 to 37 of 37

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.