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Results: 1 to 20 of 26

Tests names and labsConditionsGenes and analytesMethods

CentoColon extended panel

Centogene AG - the Rare Disease Company
Germany
1917
  • C Sequence analysis of the entire coding region

CentoCancer panel

Centogene AG - the Rare Disease Company
Germany
5231
  • C Sequence analysis of the entire coding region

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

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories
United States
844637
  • D Deletion/duplication analysis

MUTYH (MYH) Sequence Analysis

Baylor Miraca Genetics Laboratories
United States
31
  • C Sequence analysis of the entire coding region

MUTYH (MYH) Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Miraca Genetics Laboratories
United States
31
  • T Targeted variant analysis

MUTYH (MYH) Mutation Panel

Baylor Miraca Genetics Laboratories
United States
31
  • 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

Colorectal Cancer Comprehensive Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
47419
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cancer Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
1736124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

COLON, BREAST AND OVARIAN CANCER

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
3531
  • C Sequence analysis of the entire coding region

COLON CANCER

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1915
  • C Sequence analysis of the entire coding region

Adenomatous Polyposis, Familial 2 (FAP2): MYH (MUTYH) gene deletions-duplications analysis (MLPA)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • D Deletion/duplication analysis

Single gene testing MUTYH

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

CTNNB1

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

COLOTRUE™

Pathway Genomics
United States
4115
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cancer Syndrome: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
10645
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
601504
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Thyroid Cancer NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
7210
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 26

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.