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Results: 1 to 20 of 29

Tests names and labsConditionsGenes, analytes, and microbesMethods

OnkoRisk Hereditary Oncology Plus Panel

BioReference Health
United States
9777
  • C Sequence analysis of the entire coding region

OnkoRisk Women's Hereditary Cancer Panel

BioReference Health
United States
3418
  • C Sequence analysis of the entire coding region

IDH1 IDH2 Individual Marker, Brain Cancer

GoPath Diagnostics
United States
12
  • C Sequence analysis of the entire coding region

IDH1/IDH2 Mutations Analysis, Tumor

Mayo Clinic Laboratories Mayo Clinic
United States
32
  • C Sequence analysis of the entire coding region

CNS Tumor Classification by Methylation Array

Institute for Genomic Medicine (IGM) Clinical Laboratory Nationwide Children's Hospital
United States
92
  • M Methylation analysis

Cancer Hotspot Panel

Genome-Nilou Lab
Iran
4534
  • E Sequence analysis of select exons

Endeavor

PathGroup
United States
73505
  • C Sequence analysis of the entire coding region

IDH1 and IDH2 Mutation Analysis

PathGroup
United States
52
  • T Targeted variant analysis

PIK3CA variant detection

Laboratory for Molecular Pediatric Pathology Boston Children's Hospital
United States
31
  • T Targeted variant analysis

BRAF V600E variant detection

Laboratory for Molecular Pediatric Pathology Boston Children's Hospital
United States
41
  • T Targeted variant analysis

PrimBio Cancer HotSpot Panel

PrimBio Research Institute
United States
6050
  • T Targeted variant analysis

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

JAX MGMT Promoter Methylation

The Jackson Laboratory for Genomic Medicine
United States
151
  • M Methylation analysis

JAX OncoMethyl Array

The Jackson Laboratory for Genomic Medicine
United States
151
  • M Methylation analysis

Detection by FISH of del1p/del19q

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

OnkoSight Advanced CNS NGS

BioReference Health
United States
130
  • C Sequence analysis of the entire coding region

TERT Promoter Mutation Analysis

Molecular Oncology Laboratory, LabCorp
United States
22
  • T Targeted variant analysis

1p19q Deletion by FISH and IDH1 R132H Point Mutation by Immunohistochemistry with Reflex to IDH1 and IDH2 Mutation Analysis, Exon 4

ARUP Laboratories, Molecular Oncology ARUP Laboratories
United States
21
  • I Immunohistochemistry
  • E Sequence analysis of select exons

IDH1 R132H Point Mutation by Immunohistochemistry with Reflex to IDH1 and IDH2 Mutation Analysis, Exon 4

ARUP Laboratories, Molecular Oncology ARUP Laboratories
United States
21
  • I Immunohistochemistry
  • E Sequence analysis of select exons

NeoTYPE® Brain Tumor Profile

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
147
  • F Fluorescence in situ hybridization (FISH)
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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.