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Results: 21 to 40 of 60

Tests names and labsConditionsGenes, analytes, and microbesMethods

Ataxia Exome

Genetic Services Laboratory University of Chicago
United States
289481
  • C Sequence analysis of the entire coding region

Genomic Unity® Retinal Disorders Analysis

Variantyx, Inc.
United States
1394
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel 

CGC Genetics Unilabs
Portugal
1306
  • C Sequence analysis of the entire coding region

Diseases of the posterior ocular segment (WES based NGS panel of 307 gene, including CNV analysis)

CGC Genetics Unilabs
Portugal
1307
  • 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

Cerebral small vessel disease panel

CGC Genetics Unilabs
Portugal
118
  • 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

Cerebral amyloid angiopathy (sequence analysis of ITM2B 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

Hereditary Retinopathy Panel

Mendelics
Brazil
1321
  • C Sequence analysis of the entire coding region

HEREDITARY ATAXIAS EXOME PANEL

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

DEMENTIA AND ALZHEIMER EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
168
  • E Sequence analysis of select exons

ALZHEIMER AND DEMENTIA EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
168
  • E Sequence analysis of select exons

HEREDITARY AMYLOIDOSIS SYNDROME PANEL

Laboratorio de Genetica Clinica SL
Spain
122
  • E Sequence analysis of select exons

Comprehensive Eye panel

Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine
United States
1695
  • C Sequence analysis of the entire coding region

Hereditary ataxias. NGS panel of 139 genes.

Genologica Medica
Spain
220139
  • C Sequence analysis of the entire coding region

Ataxia panel. NGS panel of 157 genes.

Genologica Medica
Spain
247156
  • C Sequence analysis of the entire coding region

Dementia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
45
  • C Sequence analysis of the entire coding region

Retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 60

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.