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Results: 1 to 20 of 27 (representing 13 labs)

Tests names and labsConditionsGenes and analytesMethods

CentoCancer panel

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

Pancreatic cancer

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pancreatic Cancer Sequencing Panel

PreventionGenetics
United States
1312
  • 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

Hereditary Cancer Panel - Pancreatic14

Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center
United States
814
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Breast Plus Panel without BRCA (TP53, PTEN, CDH1, STK11, PALB2)

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
55
  • C Sequence analysis of the entire coding region

MyVantage(TM) Hereditary Comprehensive Cancer Panel

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
2434
  • C Sequence analysis of the entire coding region

PALB2 Sequencing and Deletion/Duplication

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
21
  • C Sequence analysis of the entire coding region

ONCOLOGY, PANEL

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
6780
  • C Sequence analysis of the entire coding region

Prostate Cancer Focus Panel

Fulgent Genetics
United States
5810
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ovarian Cancer Focus Panel

Fulgent Genetics
United States
5816
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Endometrial Cancer Focus Panel

Fulgent Genetics
United States
5810
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Colorectal Cancer Focus Panel

Fulgent Genetics
United States
5816
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Breast Cancer Focus Panel

Fulgent Genetics
United States
5814
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Colorectal and Gastrointestinal Cancer Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
3523
  • S Mutation scanning of the entire coding region

Focus Cancer Panel - 40 Genes

Fulgent Genetics
United States
5640
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Multi-Cancer Panel

Invitae
United States
14180
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Common Hereditary Cancers Panel (Breast, Gyn, GI)

Invitae
United States
7642
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pancreatic Cancer: Sequencing Panel and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
1515
  • C Sequence analysis of the entire coding region

Pancreatic cancer Panel

CeGaT GmbH
Germany
617
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 27

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.

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