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Results: 1 to 20 of 184

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Breast and Ovarian Cancer Panel

QDx Pathology Services, Inc.
United States
323
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clariti 20/20

QDx Pathology Services, Inc.
United States
1544
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NeXT Dx

Personalis, Inc.
United States
1413
  • I Microsatellite instability testing (MSI)
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Coffin-Siris syndrome Panel

Genetic Services Laboratory University of Chicago
United States
715
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tempus xT

Tempus AI - RTP
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

OnkoRisk Hereditary Oncology Plus Panel

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

SMARCA4 Gene Mental retardation, autosomal dominant type 16 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Hereditary Renal Cancer Panel

Mayo Clinic Laboratories Mayo Clinic
United States
119
  • C Sequence analysis of the entire coding region

Hereditary Expanded Cancer Panel

Mayo Clinic Laboratories Mayo Clinic
United States
186
  • C Sequence analysis of the entire coding region

Tempus xT

Tempus AI - CHI
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Rhabdoid Tumor Predisposition Syndrome NGS Panel

UAB Medical Genomics Laboratory UAB Medicine
United States
52
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FoundationOne® Heme

Foundation Medicine, Inc.
United States
2405
  • D Deletion/duplication analysis
  • R RNA analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Rhabdoid tumor predisposition syndrome testing (SMARCA4)

Genetic Services Laboratory University of Chicago
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Small cell carcinoma of the ovary, hypercalcemic type

Molecular Genetics Laboratory North York General Hospital
Canada
11
  • C Sequence analysis of the entire coding region

Rhabdoid predisposition syndrome

Molecular Genetics Laboratory North York General Hospital
Canada
12
  • C Sequence analysis of the entire coding region

Comprehensive cancer panel (76 genes)

Molecular Genetics Laboratory North York General Hospital
Canada
174
  • T Targeted variant analysis

NEXT GEN SEQUENCING COMPREHENSIVE SOLID TUMOR PANEL

Alverno Laboratories
United States
127
  • T Targeted variant analysis

OncoAlly™ Comprehensive Hereditary Cancer Analysis

Variantyx, Inc.
United States
188
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

OnkoSight Advanced Bladder Cancer Panel

BioReference Health
United States
139
  • C Sequence analysis of the entire coding region

Common Hereditary Cancer Screening Panel

PreventionGenetics, part of Exact Sciences
United States
9455
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 20 of 184

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.