Filters

See more specimen types...
See more states

Other countries

Results: 1 to 20 of 71 (representing 26 labs)

Tests names and labsConditionsGenes and analytesMethods

Cowden Disease and PTEN Hamartoma Tumor Syndrome

Clinical Molecular Genetics Laboratory Johns Hopkins All Children's Hospital
United States
21
  • S Mutation scanning of the entire coding region

Otogenetics Hereditary Cancers

Otogenetics
United States
3639
  • E Sequence analysis of select exons

Hereditary Cancer Panel Comprehensive

Molecular Genetics Laboratory London Health Sciences Centre
Canada
4030
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Colorectal Cancer Sequencing And Deletion/Duplication Panel

PreventionGenetics
United States
2117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cancer Sequencing and Deletion/Duplication Panel

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

Renal Cancer Sequencing Panel

PreventionGenetics
United States
2619
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PTEN Hamartoma Tumor Syndrome via the PTEN Gene

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PTEN Hamartoma Tumur Syndrome (PHTS)

Genetic Pathology SA Pathology
Australia
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PTEN-Related Disorders (Cowden syndrome, Proteus syndrome, macrocephaly and autism)

Ambry Genetics
United States
71
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Breast/Ovarian Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1618
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Breast and Ovarian Cancer High Risk Panel

Genetic Services Laboratory University of Chicago
United States
97
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Colorectal Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1021
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Colorectal Polyposis Panel

Genetic Services Laboratory University of Chicago
United States
612
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cancer Panel - Endocrine/Paraganglioma-Pheochromocytoma17

Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center
United States
717
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Hereditary Thyroid Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PTEN Sequencing and Deletion/Duplication

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
11
  • C Sequence analysis of the entire coding region

Invitae Pediatric Solid Tumors Panel

Invitae
United States
9148
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Breast Cancer STAT Panel

Invitae
United States
177
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TIMM8B

Fulgent Genetics
United States
91
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 71

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.

Support Center