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Results: 21 to 40 of 68

Tests names and labsConditionsGenes, analytes, and microbesMethods

GeneSeq: Cardio - Early-onset Coronary Artery Disease/Familial Hypercholesterolemia Panel

Integrated Genetics Westborough LabCorp
United States
712
  • C Sequence analysis of the entire coding region

GeneSeq: Cardio - Familial Hypercholesterolemia Panel

Integrated Genetics Westborough LabCorp
United States
14
  • C Sequence analysis of the entire coding region

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • 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

Familial Hypercholesterolaemia

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

Familial Hypercholesterolemia Panel, Sequencing

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
14
  • C Sequence analysis of the entire coding region

Familial Hypercholesterolemia

Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine
United States
14
  • E Sequence analysis of select exons

Horizon 274 Male

Natera, Inc.
United States
244254
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Ashkenazi Jewish Diseases

Asper Biogene Asper Biogene LLC
Estonia
4337
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hyperlipidemia NGS Panel

Fulgent Genetics
United States
1911
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Laron Syndrome (GHR Single Gene Test)

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Facial Dysostosis and Related Disorders NGS Panel

Fulgent Genetics
United States
8529
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ACMG Secondary Findings (Medically Actionable Genes, Including Cardio and Cancer) NGS Panel

Fulgent Genetics
United States
17759
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tangier Disease (ABCA1 Single Gene Test)

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hypercholesterolemia NGS Panel

Fulgent Genetics
United States
75
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Combined Pituitary Hormone Deficiency NGS Panel

Fulgent Genetics
United States
107
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hypercholesterolemia (FH) Panel

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
13
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial hypercholesterolemia (APOB, LDLR, PCSK9)

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
13
  • C Sequence analysis of the entire coding region

FAMILIAL HYPERCHOLESTEROLEMIA

Laboratorio de Genetica Clinica SL
Spain
35
  • D Deletion/duplication analysis
  • S Mutation scanning of the entire coding region
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Baylor Genetics
United States
13261
  • E Sequence analysis of select exons

Results: 21 to 40 of 68

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.