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81 genetic tests from 27 labs with tests matching your search
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Tests names and labsConditionsGenes, analytes, and microbesMethods

CETP Gene High density lipoprotein cholesterol level QTL 10 NGS Genetic DNA Test

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

[High density lipoprotein cholesterol level QTL6], 610762 (SCARB1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

[High density lipoprotein cholesterol level QTL 12], 612797 (LIPC gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • 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

High density lipoprotein cholesterol level QTL 7 (EDN1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

[High density lipoprotein cholesterol level QTL 10], 143470, Autosomal dominant (CETP gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

[High density lipoprotein cholesterol level QTL 11] (Familial lipoprotein lipase deficiency) (LPL gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

CentoNeuro Panel

CENTOGENE GmbH and LLC - Guiding Precision Medicine
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
16551199
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
971680
  • D Deletion/duplication analysis

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1101676
  • D Deletion/duplication analysis
  • 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

Leukodystrophy and Leukoencephalopathy Panel

PreventionGenetics, part of Exact Sciences
United States
202212
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Comprehensive Lipidemia Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
3325
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertriglyceridemia Gene Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
1612
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dystonia Exome

Genetic Services Laboratory, University of Chicago
United States
93170
  • C Sequence analysis of the entire coding region

SCARB1 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Epilepsy

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
414800
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Plus Panel

Fulgent Genetics
United States
716335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
81 tests from 27 labs
See all labs
View the list of labs matching your search query.
More help
❮Page 1 of 5❯
CETP Gene High density lipoprotein cholesterol level QTL 10 NGS Genetic DNA Test by DNA Labs India
1 condition, 1 gene
[High density lipoprotein cholesterol level QTL6], 610762 (SCARB1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
[High density lipoprotein cholesterol level QTL 12], 612797 (LIPC gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Clinical Exome by Fulgent Genetics
5128 conditions, 4672 genes
High density lipoprotein cholesterol level QTL 7 (EDN1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
[High density lipoprotein cholesterol level QTL 10], 143470, Autosomal dominant (CETP gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
[High density lipoprotein cholesterol level QTL 11] (Familial lipoprotein lipase deficiency) (LPL gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes
MVL Vision Panel by Molecular Vision Laboratory
1655 conditions, 1199 genes
Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel by Labcorp Genetics (formerly Invitae), LabCorp
971 conditions, 680 genes
Nuclear-Mito NGS Panel by Fulgent Genetics
1101 conditions, 676 genes
Inherited Metabolic Disorders Panel by Dhiti Omics Technologies Private Ltd
376 conditions, 317 genes
Leukodystrophy and Leukoencephalopathy Panel by PreventionGenetics, part of Exact Sciences
202 conditions, 212 genes
Invitae Comprehensive Lipidemia Panel by Labcorp Genetics (formerly Invitae), LabCorp
33 conditions, 25 genes
Intellectual Disability NGS Panel by Fulgent Genetics
1058 conditions, 554 genes
Hypertriglyceridemia Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
16 conditions, 12 genes
Dystonia Exome by Genetic Services Laboratory, University of Chicago
93 conditions, 170 genes
SCARB1 Single Gene by Fulgent Genetics
1 condition, 1 gene
Comprehensive Epilepsy by MNG Laboratories (Medical Neurogenetics, LLC.)
414 conditions, 800 genes
Beacon Expanded Female Carrier Screening Plus Panel by Fulgent Genetics
716 conditions, 335 genes

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.