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Results: 1 to 18 of 18

Tests names and labsConditionsGenes, analytes, and microbesMethods

HSPG2 Gene Schwartz-Jampel syndrome type 1 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

A2M Gene Alpha-2-macroglobulin deficiency NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Alpha-2-macroglobulin deficiency, 614036, Autosomal dominant; A2MD (A2M gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Alzheimer disease, susceptibility to, 104300, Autosomal dominant (Early-onset autosomal dominant Alzheimer disease) (A2M 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

Alpha-2-macroglobulin deficiency, 614036, Autosomal dominant; A2MD (A2M 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

qGenEx Intellectual disability

Quantitative Genomic Medicine Laboratories, SL
Spain
31969
  • S Mutation scanning of the entire coding region
  • 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

Alpha-2-macroglobulin deficiency (sequence analysis of A2M gene)

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

Alzheimer's panel

Genologica Medica
Spain
2510
  • C Sequence analysis of the entire coding region

Alzheimer's panel. NGS panel of 10 genes.

Genologica Medica
Spain
2510
  • C Sequence analysis of the entire coding region

Alzheimer y demencia

Bioarray
Spain
125
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Comprehensive Dementia (NGS Panel and Copy Number Analysis)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
10145
  • C Sequence analysis of the entire coding region

ALZHEIMER DISEASE, LATE-ONSET

Laboratorio de Genetica Clinica SL
Spain
22
  • X Mutation scanning of select exons

Platelet Disorders

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
1255
  • C Sequence analysis of the entire coding region

A2M Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • 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

Results: 1 to 18 of 18

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.