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Results: 1 to 20 of 23

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
6021038
  • C Sequence analysis of the entire coding region

Apolipoprotein E deficiency

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

APOE, APP, PSEN1, PSEN2. NextGeneDx.Complete sequencing by NGS

Instituto de Medicina Genomica
Spain
44
  • C Sequence analysis of the entire coding region

Early-onset autosomal dominant Alzheimer disease

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Alzheimer disease (NGS panel for 8 genes)

CGC Genetics
Portugal
58
  • C Sequence analysis of the entire coding region

Alzheimer disease type 2 (APOE gene, alleles E2, E3 and E4)

CGC Genetics
Portugal
11
  • T Targeted variant analysis

Single gene testing APOE

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

APOE

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ADmark® ApoE Genotype Analysis and Interpretation (Symptomatic)

Athena Diagnostics Inc Quest Diagnostics
United States
11
  • T Targeted variant analysis

Sudden Death Syndrome NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
18568
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Parkinson-Alzheimer-Dementia NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
8237
  • D Deletion/duplication analysis
  • C 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 Cancer NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
256112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Apolipoprotein E deficiency

MedGene
Slovakia
11
  • E Sequence analysis of select exons

Pan-Cardio NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
239101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Apolipoprotein E deficiency

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

APOE: ApoE gene genotyping

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Alzheimer: MAPT, CLU, PICALM, CR1 genes screening

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
44
  • X Mutation scanning of select exons

Alzheimer: Apo-E, PSEN1, PSEN2, APP, A2M and MAPT genes sequence analysis (select exons)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
46
  • C Sequence analysis of the entire coding region

Alzheimer: Apo-E, PSEN1, PSEN2, A2M and APP genes sequence analysis (select exons)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
45
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 23

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.