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Results: 161 to 180 of 183

Tests names and labsConditionsGenes, analytes, and microbesMethods

Defects of phagocytosis Panel

CeGaT GmbH
Germany
3759
  • C Sequence analysis of the entire coding region

Syndromes with immunodeficiency Panel

CeGaT GmbH
Germany
3338
  • C Sequence analysis of the entire coding region

Bone marrow failure syndromes Panel

CeGaT GmbH
Germany
1537
  • C Sequence analysis of the entire coding region

WAS Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Wiskott-Aldrich syndrome

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

Severe congenital neutropenia X-linked

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

Wiskott-Aldrich syndrome, WAS sequencing

Molecular Diagnostics Laboratory Seoul National University Hospital
South Korea
11
  • C Sequence analysis of the entire coding region

Wiskott-aldrich syndrome

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
11
  • C Sequence analysis of the entire coding region

WAS Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • D Deletion/duplication analysis

WAS Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Inherited Neutropenia panel by next-generation sequencing (NGS)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
3940
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Clinical Exome

Fulgent Genetics
United States
51284672
  • 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

Severe Congenital Neutropenia Sequential Panel

FirmaLab
United States
15
  • C Sequence analysis of the entire coding region

Thrombocytopenia 1

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

Wiskott-Aldrich syndrome

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

Neutropenia, severe congenital

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

Wiskott-Aldrich syndrome

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

Thrombocytopenia 1

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

Neutropenia, severe congenital

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

Results: 161 to 180 of 183

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.