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Results: 21 to 40 of 69 (representing 24 labs)

Tests names and labsConditionsGenes and analytesMethods

Hereditary Brain, CNS, PNS Cancer Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
4317
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fanconi Anemia

Asper Biogene Asper Biogene LLC
Estonia
1717
  • 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

BRCA1, BRCA2, and PALB2 Mutation Analysis

Genetic Services Laboratory University of Chicago
United States
63
  • 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

Invitae Bone Marrow Failure Syndromes Panel

Invitae
United States
4939
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fanconi Anemia Comprehensive Panel

Fulgent Genetics
United States
20017
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Breast Cancer Comprehensive Panel

Fulgent Genetics
United States
51518
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cancer Panel

Fulgent Genetics
United States
1735124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pancreatic Cancer Comprehensive Panel

Fulgent Genetics
United States
61322
  • 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

Fanconi anemia

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1416
  • 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

PALB2 - Gene Sequencing & Del/Dup analysis

Genome Diagnostics VU University Medical Center
Netherlands
21
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • T Targeted variant analysis

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

Single gene testing PALB2

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Breast and Ovarian Cancer: Sequencing and Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
1819
  • C Sequence analysis of the entire coding region

Renal Cancer: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
1111
  • C Sequence analysis of the entire coding region

Fanconi anemia Panel

CeGaT GmbH
Germany
1716
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 69

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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