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Results: 41 to 60 of 92

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae First Tier Population Screen

Invitae
United States
1011
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Carrier Screen

Invitae
United States
886547
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Heart Health Test

Color Diagnostics, LLC DBA Color Health
United States
1930
  • C Sequence analysis of the entire coding region

Familial Hypercholesterolemia: LDLR Deletion/Duplication MLPA

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
11
  • D Deletion/duplication analysis

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
328300
  • C Sequence analysis of the entire coding region

LDLR MLPA

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • D Deletion/duplication analysis

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • C Sequence analysis of the entire coding region

Dyslipidemia and early atherosclerosis panel. 84-gene NGS panel.

Genologica Medica
Spain
13384
  • C Sequence analysis of the entire coding region

Familial hypercholesterolemia panel. 16-gene NGS panel.

Genologica Medica
Spain
2016
  • C Sequence analysis of the entire coding region

Hyperlipidemia panel. 18-gene NGS panel.

Genologica Medica
Spain
2518
  • C Sequence analysis of the entire coding region

Familial Amyloidosis

Genologica Medica
Spain
4419
  • C Sequence analysis of the entire coding region

Hyperlipidemia panel

Genologica Medica
Spain
54
  • C Sequence analysis of the entire coding region

Preventive 59

Genologica Medica
Spain
17259
  • C Sequence analysis of the entire coding region

FAMILIAL HYPERCHOLESTEROLEMIA GENETIC PANEL

Duzen Laboratories Duzen BBAGUAS
Turkey
44
  • C Sequence analysis of the entire coding region

Familial Hypercholesterolaemia

Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center
Turkey
11
  • C Sequence analysis of the entire coding region

Amyloid Related Disorders (NGS Panel and Copy Number Analysis)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
516
  • C Sequence analysis of the entire coding region

FAMILIAL HYPERCHOLESTEROLEMIA LDLR

BioReference Health
United States
11
  • T Targeted variant analysis

OncoGeneDx Custom Panel

GeneDx
United States
10382
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Horizon 106 plus TSE

Natera, Inc.
United States
103107
  • E Enzyme assay
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Horizon 106

Natera, Inc.
United States
103106
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 41 to 60 of 92

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.