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Results: 1 to 16 of 16

Tests names and labsConditionsGenes, analytes, and microbesMethods

Myeloproliferative disorder with eosinophilia, 131440, Autosomal dominant (Unclassified chronic myeloproliferative disease) (PDGFRB gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Solid Tumor Panel

Centogene AG - the Rare Disease Company
Germany
218135
  • C Sequence analysis of the entire coding region

Myeloid Tumor Panel

Centogene AG - the Rare Disease Company
Germany
7434
  • C Sequence analysis of the entire coding region

PDGFRB - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
971680
  • D Deletion/duplication analysis

Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel

PreventionGenetics, part of Exact Sciences
United States
346160
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Overgrowth Syndromes Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
9653
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Detection by FISH of PDGFRB (5q32) rearrangements

CGC Genetics Unilabs
Portugal
11
  • F Fluorescence in situ hybridization (FISH)

Parkinson's disease panel. NGS panel of 22 genes.

Genologica Medica
Spain
4522
  • C Sequence analysis of the entire coding region

Dystonia panel. NGS panel of 20 genes.

Genologica Medica
Spain
3520
  • C Sequence analysis of the entire coding region

PDGFRB gene mutations

Duzen Laboratories Duzen BBAGUAS
Turkey
41
  • T Targeted variant analysis

PDGFRB Single Gene

Fulgent Genetics
United States
811
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FISH - HEMATOLOGY | ONCOLOGY | LYMPHOMA

Warren G. Sanger Human Genetics Laboratory Nebraska Medicine (formerly a UNMC Lab)
United States
1054
  • F Fluorescence in situ hybridization (FISH)

Eosinophilia IFISH Panel

Cytogenetics Laboratory University of Washington
United States
14
  • I FISH-interphase

Platelets, Coagulation disorders Panel

CeGaT GmbH
Germany
1717
  • 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: 1 to 16 of 16

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.