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Results: 1 to 20 of 48 (representing 27 labs)

Tests names and labsConditionsGenes and analytesMethods

FoundationOne®

Foundation Medicine, Inc.
United States
1315
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Tempus xO assay

Tempus Labs, Inc.
United States
11714
  • R RNA analysis
  • C Sequence analysis of the entire coding region

OmniSeq Comprehensive

OmniSeq OmniSeq, Inc.
United States
1144
  • D Deletion/duplication analysis
  • R RNA analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

FoundationOne® Heme

Foundation Medicine, Inc.
United States
2405
  • D Deletion/duplication analysis
  • R RNA analysis
  • E Sequence analysis of select exons
  • 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

Leukoencephalopathy, diffuse hereditary, with spheroids

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

NeoTYPE® Discovery Profile for Solid Tumors

NeoGenomics Laboratories NeoGenomics Laboratories, Inc.
United States
1315
  • I Immunohistochemistry
  • F Fluorescence in situ hybridization (FISH)
  • C Sequence analysis of the entire coding region

Tempus xT assay

Tempus Labs, Inc.
United States
2592
  • I Microsatellite instability testing (MSI)
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Providence Personalized Medicine Panel - Solid Tumor

Providence Regional Laboratories Providence Health and Services
United States
1308
  • C Sequence analysis of the entire coding region

152 Integrated Advantage NGS Solid Tumor Panel

Integrated Molecular Diagnostics Pathology, Inc.
United States
6152
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Dystonia Exome Panel

Genetic Services Laboratory University of Chicago
United States
93170
  • C Sequence analysis of the entire coding region

Comprehensive Panel for Individualized Cancer Threatment

GeneKor MSA
Greece
1652
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • E Sequence analysis of select exons
  • T Targeted variant analysis

CSF1R. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • -- Sequence analysis of the entire coding region

DEMENTIA & ALZHEIMER: NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
1614
  • C Sequence analysis of the entire coding region

Diffuse Leukoencephalopathy with Spheroids, Sequencing CSF1R Gene

Reference Laboratory Genetics
Spain
11
  • -- Sequence analysis of the entire coding region

Leukoencephalopathy, diffuse hereditary, with spheroids

LifeLabs Genetics
Canada
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dementia Panel

Blueprint Genetics
Finland
217
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Epilepsy Panel

Blueprint Genetics
Finland
4194
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Leukodystrophy and Leukoencephalopathy Panel

Blueprint Genetics
Finland
242
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 48

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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