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Results: 1 to 20 of 20 (representing 9 labs)

Tests names and labsConditionsGenes and analytesMethods

Comprehensive Neuropathy NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
8271
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Sensory and Autonomic Neuropathy NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
1212
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Hereditary Sensory and Autonomic Neuropathy Panel

Invitae
United States
1817
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Neuropathies Panel

Invitae
United States
10779
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary spastic paraplegia (HSP), autosomal dominant and X-linked Panel

CeGaT GmbH
Germany
2217
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies Panel Sequencing

ARUP Laboratories, Molecular Genetics and Genomics
United States
3478
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth (CMT) and Related Hereditary Neuropathies, PMP22 Deletion/Duplication with Reflex to Sequencing Panel

ARUP Laboratories, Molecular Genetics and Genomics
United States
3478
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing ATL1

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
147143
  • -- Sequence analysis of the entire coding region

ATL1

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charcot Marie Tooth Disease Extended NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
11549
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ATL1

Medizinisch Genetisches Zentrum München MGZ München
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ATL1 (HSAN) DNA Sequencing Test

Athena Diagnostics Inc
United States
11
  • C Sequence analysis of the entire coding region

Hereditary Neuropathies: Sequencing Panel

Emory Genetics Laboratory Emory University School of Medicine
United States
12386
  • 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

Spastic Paraplegia NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
4525
  • -- Deletion/duplication analysis
  • -- Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
752392
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Neuropathies NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
9033
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary spastic paraplegia type 3

Human Genetics Ruhr University
Germany
21
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

hereditary spastic paraplegia type 31

Human Genetics Ruhr University
Germany
21
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 20

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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