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Results: 21 to 40 of 84

Tests names and labsConditionsGenes, analytes, and microbesMethods

Frontotemporal lobar degeneration, TARDBP-related, 612069, Autosomal dominant (Frontotemporal dementia with motor neuron disease) (TARDBP gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Genomic Unity Motor Neuron Disorders Analysis (includes AR, C9ORF72 STR analysis)

Variantyx, Inc.
United States
14118
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Parkinson Disease and Parkinsonism Panel

PreventionGenetics, part of Exact Sciences
United States
7071
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Amyotrophic lateral sclerosis and related disorders NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
124
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Amyotrophic lateral sclerosis and related disorders Deletion/ Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis and related disorders Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Frontotemporal Dementia Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
2913
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis/Motor Neuron Disease via the TARDBP Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TARDBP

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis/motor neuron disease (WES based NGS panel of 30 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
130
  • C Sequence analysis of the entire coding region

Neurodegenerative panel _v.2.0

CGC Genetics Unilabs
Portugal
15207
  • C Sequence analysis of the entire coding region

Hereditary dementias (WES based NGS panel of 44 genes, including analysis of CNVs)

CGC Genetics Unilabs
Portugal
144
  • C Sequence analysis of the entire coding region

Frontotemporal dementia (WES based NGS panel of 20 genes, including analysis of CNVs)

CGC Genetics Unilabs
Portugal
120
  • C Sequence analysis of the entire coding region

Alzheimer's and other dementias panel_v.2.0

CGC Genetics Unilabs
Portugal
120
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis 10 (sequence analysis of TARDBP gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Dementia and Parkinson's Panel

Mendelics
Brazil
260
  • C Sequence analysis of the entire coding region

Spastic Paraplegia and Amyotrophic Lateral Sclerosis Panel

Mendelics
Brazil
260
  • C Sequence analysis of the entire coding region

AMYOTROPHIC LATERAL SCLEROSIS EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
157
  • E Sequence analysis of select exons

PARKINSON'S DISEASE AND PARKINSONISM EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
196
  • E Sequence analysis of select exons

HEREDITARY ATAXIAS EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
11202
  • E Sequence analysis of select exons

Results: 21 to 40 of 84

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.