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Results: 21 to 38 of 38

Tests names and labsConditionsGenes, analytes, and microbesMethods

BCR/ABL, expanded JAK2

PathGroup
United States
113
  • T Targeted variant analysis

BCR/ABL, JAK2 V617F, MPL

PathGroup
United States
83
  • T Targeted variant analysis

BCR/ABL, expanded JAK2, MPL

PathGroup
United States
115
  • T Targeted variant analysis

BCR/ABL Quant Non-CML, CALR and JAK2 V617F Mutation Detect and Quant

PathGroup
United States
104
  • T Targeted variant analysis

Congenital Limb Malformation Panel

PreventionGenetics, part of Exact Sciences
United States
10399
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Calreticulin, Exon 9 Mutation Analysis

UCSF Molecular Diagnostics Laboratory University of California, San Francisco
United States
11
  • X Mutation scanning of select exons
  • E Sequence analysis of select exons

Hereditary Thrombocythemia via the THPO Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Platelet Disorder NGS Panel

Fulgent Genetics
United States
7444
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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

Erythrocytosis NGS Panel

Fulgent Genetics
United States
6124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CALR Exon 9 Mutation Analysis

Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories
United States
31
  • T Targeted variant analysis

JAK2 V617F Mutation Testing

Tulane Hayward Genetics Center Molecular Diagnostics Lab Tulane University
United States
51
  • T Targeted variant analysis

THPO Single Gene

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

SH2B3 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CALR Single Gene

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

Myelofibrosis NGS Panel

Fulgent Genetics
United States
84
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS Panel

Fulgent Genetics
United States
543178
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 38 of 38

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.