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Results: 1 to 20 of 112

Tests names and labsConditionsGenes, analytes, and microbesMethods

geneType for melanoma

Phenogen Sciences Laboratories Phenogen Sciences Inc.
Australia
11
  • T Targeted variant analysis

Hereditary Prostate Cancer Panel

QDx Pathology Services, Inc.
United States
416
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Melanoma Cancer Panel

QDx Pathology Services, Inc.
United States
43
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Pancreatic Cancer Panel

Clariti Diagnostics Laboratories LLC
United States
415
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Melanoma Cancer Panel

Clariti Diagnostics Laboratories LLC
United States
43
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NGS Panel for Dyskeratosis congenita

BloodGenetics
Spain
1216
  • C Sequence analysis of the entire coding region

Invitae Expanded Renal Disease Panel

Invitae
United States
693388
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae eMERGE Panel

Invitae
United States
5916
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NGS Panel for Bone Marrow failure

BloodGenetics
Spain
5769
  • C Sequence analysis of the entire coding region

Solid Tumor Panel

Centogene AG - the Rare Disease Company
Germany
218135
  • C Sequence analysis of the entire coding region

STK11 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Multi-Cancer + RNA Panel

Invitae
United States
14363
  • D Deletion/duplication analysis

Invitae Common Hereditary Cancers + RNA Panel

Invitae
United States
11447
  • D Deletion/duplication analysis

Invitae eMERGE Panel

Invitae
United States
5916
  • D Deletion/duplication analysis

Invitae RASopathies and Noonan Spectrum Disorders Panel

Invitae
United States
6028
  • D Deletion/duplication analysis

CancerNext® 37

Ambry Genetics
United States
7937
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Variant Resolution Test for CancerNext® 37 (+RNAinsight®)

Ambry Genetics
United States
7918
  • D Deletion/duplication analysis
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Variant Resolution Test for Penn Cancer Grant Panel (+RNAinsight®)

Ambry Genetics
United States
7918
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Penn Cancer Grant Panel

Ambry Genetics
United States
7980
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BRCANext-Expanded™

Ambry Genetics
United States
3520
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 112

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.