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Results: 21 to 40 of 41

Tests names and labsConditionsGenes, analytes, and microbesMethods

Neutropenia

Asper Biogene Asper Biogene LLC
Estonia
3326
  • C Sequence analysis of the entire coding region

RAC2 - Genetic Analysis

Versiti Diagnostic Laboratories Versiti, Inc
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
9562
  • C Sequence analysis of the entire coding region

Neutropenia Panel, Chronic

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
2315
  • C Sequence analysis of the entire coding region

B-Negative Severe Combined Immunodeficiency NGS Panel

Fulgent Genetics
United States
7313
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bone Marrow Failure NGS Panel

Fulgent Genetics
United States
18060
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Severe Combined Immunodeficiency NGS Panel

Fulgent Genetics
United States
33090
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neutropenia NGS Panel

Fulgent Genetics
United States
3921
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Severe Congenital Neutropenia (Extended Panel) , Panel Massive Sequencing (NGS) 20 Genes

Reference Laboratory Genetics
Spain
2220
  • C Sequence analysis of the entire coding region

Severe Congenital Neutropenia , Panel Massive Sequencing (NGS) 9 Genes

Reference Laboratory Genetics
Spain
109
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Related Disorders , Panel Massive Sequencing (NGS) 59 Genes

Reference Laboratory Genetics
Spain
6358
  • C Sequence analysis of the entire coding region

Severe Congenital Neutropenia Gene Set

Clinical Genomics Laboratory Washington University in St. Louis
United States
2848
  • C Sequence analysis of the entire coding region

Defects of phagocytosis Panel

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

RAC2 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

RAC2 Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • D Deletion/duplication analysis

RAC2 Single Gene

Fulgent Genetics
United States
11
  • 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
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Severe Combined Immunodeficiency and T Cell Disorders 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
3541
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 41

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.