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Results: 41 to 54 of 54

Tests names and labsConditionsGenes, analytes, and microbesMethods

HYPERLIPOPROTEINEMIA TYPE 1

Laboratorio de Genetica Clinica SL
Spain
44
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

APOLIPOPROTEIN C2 DEFICIENCY

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Dyslipidemia NGS panel (29 genes), Sequence & CNV analysis

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
929
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pancreatitis Panel

Blueprint Genetics
Finland
29
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperlipidemia Panel

Blueprint Genetics
Finland
118
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Apo CII deficiency

Department of Endocrinology and Metabolism Okinaka Memorial Institute for Medical Research
Japan
11
  • C Sequence analysis of the entire coding region

Familial apolipoprotein C-II deficiency

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

Chylomicronemia

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
15
  • C Sequence analysis of the entire coding region

APOC2 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

APOC2 Single Gene

Fulgent Genetics
United States
11
  • 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

Hypertriglyceridemia

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
116
  • C Sequence analysis of the entire coding region

Hypertriglyceridaemia genetic screen

Cardiovascular Genetics Laboratory PathWest Laboratory Medicine WA - Fiona Stanley Hospital
Australia
27
  • C Sequence analysis of the entire coding region

Apolipoprotein C2 deficiency

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 54 of 54

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.