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Results: 21 to 40 of 40

Tests names and labsConditionsGenes, analytes, and microbesMethods

Dementia panel. NGS panel of 21 genes.

Genologica Medica
Spain
4421
  • C Sequence analysis of the entire coding region

Polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
22
  • C Sequence analysis of the entire coding region

Osteolysis and Related Disorders , Panel Massive Sequencing (NGS) 6 Genes

Reference Laboratory Genetics
Spain
56
  • C Sequence analysis of the entire coding region

Leukodystrophies , Panel Massive Sequencing (NGS) 57 genes

Reference Laboratory Genetics
Spain
6056
  • C Sequence analysis of the entire coding region

NASU-HAKOLA DISEASE (POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA)

Laboratorio de Genetica Clinica SL
Spain
12
  • C Sequence analysis of the entire coding region

Nasu-Hakola Disease , Sequencing TREM2 Gene

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

Nasu-Hakola Disease , Sequencing TYROBP Gene

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

NGS panel - dementia/ALS

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
4254
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Single gene testing TREM2

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Single gene testing TYROBP

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Dementia all Panel

CeGaT GmbH
Germany
3236
  • C Sequence analysis of the entire coding region

Basal ganglia calcification Panel

CeGaT GmbH
Germany
5227
  • C Sequence analysis of the entire coding region

Frontotemporal Dementia (FTD) Panel

CeGaT GmbH
Germany
2928
  • C Sequence analysis of the entire coding region

TREM2 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TYROBP Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS Panel

Fulgent Genetics
United States
543178
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • 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

Leukoencephalopathy NGS Panel

Fulgent Genetics
United States
15569
  • 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

Results: 21 to 40 of 40

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.