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Results: 21 to 40 of 93

Tests names and labsConditionsGenes, analytes, and microbesMethods

PrimBio Cancer HotSpot Panel

PrimBio Research Institute
United States
6050
  • T Targeted variant analysis

Hereditary Myeloid Malignancy Panel

Genetic Services Laboratory University of Chicago
United States
3785
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TP53 sequencing and deletion/duplication

Children's Hospital of Los Angeles, Center for Personalized Medicine
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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

Primbio Breast Cancer Therapy Panel

PrimBio Research Institute
United States
52
  • C Sequence analysis of the entire coding region

myRisk Single Site Analysis

Myriad Genetics, Inc.
United States
3245
  • T Targeted variant analysis

PIC3CA, 5 or 11 mutations

GENOTYPOS MSA
Greece
21
  • T Targeted variant analysis

PIK3CA Mutation Analysis, Breast Cancer, IVD

Molecular Oncology Laboratory, LabCorp
United States
11
  • T Targeted variant analysis

Breast Cancer Prognostic Gene Signature Assay (Prosigna®), IVD

Molecular Oncology Laboratory, LabCorp
United States
11
  • T Targeted variant analysis

OncoGeneDx Custom Panel

GeneDx
United States
10382
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Common Cancer Management Panel

GeneDx
United States
5637
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Breast Cancer Management Panel

GeneDx
United States
249
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Breast/Gyn Cancer Panel

GeneDx
United States
4624
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Common Cancer Panel

GeneDx
United States
6047
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Schwannomatosis NGS Panel

Fulgent Genetics
United States
857
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy NGS Panel

Fulgent Genetics
United States
450128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan and RASopathies NGS Panel

Fulgent Genetics
United States
23526
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pachyonychia Congenita NGS Panel

Fulgent Genetics
United States
228
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Heart Defect NGS Panel

Fulgent Genetics
United States
377114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 93

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.