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Results: 81 to 93 of 93

Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sudden Death Syndrome NGS Panel

Fulgent Genetics
United States
16868
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FTD - ALS panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
2815
  • C Sequence analysis of the entire coding region

Parkinson-Alzheimer-Dementia NGS Panel

Fulgent Genetics
United States
7739
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Glaucoma NGS Panel

Fulgent Genetics
United States
6826
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis NGS Panel

Fulgent Genetics
United States
8443
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Frontotemporal Dementia

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Dementia, frontotemporal, with or without parkinsonism

MedGene
Slovakia
11
  • E Sequence analysis of select exons

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Frontotemporal Dementia

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Dementia, frontotemporal, with or without parkinsonism

Praxis fuer Humangenetik Wien
Austria
11
  • E Sequence analysis of select exons

C9orf72-Related Amyotrophic Lateral Sclerosis/Frontotemporal Dementia

MGZ Medical Genetics Center
Germany
21
  • T Targeted variant analysis

Frontotemporal Dementia (MAPT and GRN)

MVZ Dr. Eberhard & Partner Dortmund
Germany
22
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Results: 81 to 93 of 93

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.