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Results: 1 to 20 of 73

Tests names and labsConditionsGenes and analytesMethods

KIT, selective sequencing of exons 8, 9, 11, 13 and 17

Centogene AG - the Rare Disease Company
Germany
51
  • T Targeted variant analysis

Solid Tumor Panel

Centogene AG - the Rare Disease Company
Germany
4062
  • C Sequence analysis of the entire coding region

Cancer Hotspot Panel

Centogene AG - the Rare Disease Company
Germany
4688
  • E Sequence analysis of select exons

Myeloid Tumor Panel

Centogene AG - the Rare Disease Company
Germany
3253
  • X Mutation scanning of select exons

Gastrointestinal stromal tumor, somatic

Centogene AG - the Rare Disease Company
Germany
11
  • C Sequence analysis of the entire coding region

cKIT Mutation by Sequencing

Cancer Genetics, Inc.
United States
21
  • E Sequence analysis of select exons

Gastrointestinal stromal tumor, somatic

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Gastrointestinal stromal tumor

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KIT Sequencing of Selected Exons

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
11
  • X Mutation scanning of select exons

Comprehensive Panel for Individualized Cancer Threatment

GeneKor MSA
Greece
1652
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • E Sequence analysis of select exons
  • T Targeted variant analysis

Hereditary Gastric Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1019
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

KIT. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Cancer NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
4335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories
United States
845637
  • D Deletion/duplication analysis

Piebaldism and Familial Gastrointestinal Stromal Tumors (GISTs) via the KIT Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Familial Gastrointestinal Stromal Tumors (GISTs) via the PDGFRA Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

nucSEEK® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KIT related disorders - KIT Sequencing

Molecular Genetics Laboratory Children's Hospital Colorado
United States
51
  • C Sequence analysis of the entire coding region

Gastro-intestinal Stromal Tumour (KIT & PDGFRA)

Genomic Diagnostics Laboratory Central Manchester NHS Foundation Trust
United Kingdom
12
  • T Targeted variant analysis

Results: 1 to 20 of 73

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.