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Labs matching your search

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33 labs with tests matching your search
Lab name Tests matching your search
Amsterdam UMC Genome Diagnostics Netherlands2
Baylor Genetics United States13
Bioarray Spain1
Biochemical Genetics Laboratory United States1
Blueprint Genetics Finland4
CEN4GEN Institute for Genomics and Molecular Diagnostics Canada1
CENTOGENE GmbH and LLC - Guiding Precision Medicine Germany1
CGC Genetics Portugal3
CNH Molecular Diagnostics Laboratory United States1
CeGaT GmbH Germany2
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory United States2
Clinical Biochemical Genetics Diagnostic Laboratory United States1
DNA Labs India India2
Dep. of Paediatrics and Inherited Metabolic Disorders Czech Republic1
Dhiti Omics Technologies Private Ltd India1
Fulgent Genetics United States19
GeneDx United States5
Genetic Services Laboratory United States1
Integrated Genetics Westborough United States6
Intergen Genetics and Rare Diseases Diagnosis Center Turkey2
Johns Hopkins Genomics DNA Diagnostic Laboratory United States1
Labcorp Genetics (formerly Invitae) United States8
Laboratorio de Genetica Clinica SL Spain7
MGZ Medical Genetics Center Germany4
Mayo Clinic Laboratories United States6
Mendelics Brazil2
Molecular Vision Laboratory United States3
Myriad Genetics, Inc. United States2
PreventionGenetics, part of Exact Sciences United States6
Quantitative Genomic Medicine Laboratories, SL Spain2
Revvity Omics United States1
Translational Metabolic Laboratory Netherlands1
Variantyx, Inc. United States1
Results:
113 genetic tests from 33 labs with tests matching your search
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Compare between 2 to 5 tests using the icon in the search results to make your selection.
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Download data for all or selected tests, using the check boxes in the search results to make your selection.
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51274672
  • D Deletion/duplication analysis
  • 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
16541199
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism NGS Panel

Fulgent Genetics
United States
602355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1101676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Invitae Nuclear Mitochondrial Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
394319
  • 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

Invitae Comprehensive Neurometabolic Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
351249
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Metabolic Newborn Screening Confirmation Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
201158
  • D Deletion/duplication analysis
  • 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

Beacon Expanded Male Carrier Screening Panel

Fulgent Genetics
United States
636298
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Plus Panel

Fulgent Genetics
United States
661306
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • 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

Mitochondrial genome sequencing

Molecular Vision Laboratory
United States
524339
  • C Sequence analysis of the entire coding region

Hypoglycemia Panel

PreventionGenetics, part of Exact Sciences
United States
217171
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Hypoglycemia Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
173119
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
325300
  • C Sequence analysis of the entire coding region

Invitae Hyperammonemia Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
7572
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
113 tests from 33 labs
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❮Page 1 of 6❯
Clinical Exome by Fulgent Genetics
5127 conditions, 4672 genes
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes
MVL Vision Panel by Molecular Vision Laboratory
1654 conditions, 1199 genes
Comprehensive Metabolism NGS Panel by Fulgent Genetics
602 conditions, 355 genes
Nuclear-Mito NGS Panel by Fulgent Genetics
1101 conditions, 676 genes
MitoMet®Plus aCGH Analysis by Baylor Genetics
842 conditions, 637 genes
Invitae Nuclear Mitochondrial Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
394 conditions, 319 genes
Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel by Labcorp Genetics (formerly Invitae), LabCorp
971 conditions, 680 genes
Invitae Comprehensive Neurometabolic Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
351 conditions, 249 genes
Invitae Metabolic Newborn Screening Confirmation Panel by Labcorp Genetics (formerly Invitae), LabCorp
201 conditions, 158 genes
Beacon Expanded Female Carrier Screening Plus Panel by Fulgent Genetics
716 conditions, 335 genes
Beacon Expanded Male Carrier Screening Panel by Fulgent Genetics
636 conditions, 298 genes
Beacon Expanded Male Carrier Screening Plus Panel by Fulgent Genetics
661 conditions, 306 genes
Beacon Expanded Female Carrier Screening Panel by Fulgent Genetics
690 conditions, 326 genes
Inherited Metabolic Disorders Panel by Dhiti Omics Technologies Private Ltd
376 conditions, 317 genes
Mitochondrial genome sequencing by Molecular Vision Laboratory
524 conditions, 339 genes
Hypoglycemia Panel by PreventionGenetics, part of Exact Sciences
217 conditions, 171 genes
Invitae Hypoglycemia Panel by Labcorp Genetics (formerly Invitae), LabCorp
173 conditions, 119 genes
qCarrier Plus by Quantitative Genomic Medicine Laboratories, SL
325 conditions, 300 genes
Invitae Hyperammonemia Panel by Labcorp Genetics (formerly Invitae), LabCorp
75 conditions, 72 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.