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New filters have been added to narrow your search: Test target, to filter by number of genes; Genes and Conditions, to search by gene symbol or condition name; and Labs, to search by a laboratory name.
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Glycogen storage disease, type IV
Synonyms: AMYLOPECTINOSIS; ANDERSEN DISEASE; BRANCHER DEFICIENCY; CIRRHOSIS, FAMILIAL, WITH DEPOSITION OF ABNORMAL GLYCOGEN; GBE1 DEFICIENCY; GLYCOGEN BRANCHING ENZYME DEFICIENCY; GLYCOGENOSIS IV; GSD IV; Glycogen storage disease due to glycogen branching enzyme deficiency
Gene: GBE1

Labs matching your search

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46 labs with tests matching your search, 4 labs matching in other ways
Lab name Tests matching your search
ARUP Laboratories, Molecular Genetics and Genomics United States2
Ambry Genetics United States2
Amsterdam UMC, Location AMC Netherlands1
Baylor Genetics United States6
Bioarray Spain1
Blueprint Genetics Finland2
CEN4GEN Institute for Genomics and Molecular Diagnostics Canada3
CENTOGENE GmbH and LLC - Guiding Precision Medicine Germany1
CGC Genetics Portugal1
CNH Molecular Diagnostics Laboratory United States9
CeGaT GmbH Germany3
Center for Human Genetics Belgium1
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory United States6
DDC Clinic Molecular Diagnostics Laboratory United States1
Dhiti Omics Technologies Private Ltd India1
Dubai Health Genomic Medicine Center United Arab Emirates1
Duzen Laboratories Turkey2
Fulgent Genetics United States35
GeneDx United States2
GeneID Lab - Advanced Molecular Diagnostics United States1
Genesys Diagnostics United States3
Genetic Services Laboratory United States3
Genome-Nilou Lab Iran1
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics United States1
Greenwood Genetic Center Diagnostic Laboratories United States3
HNL Genomics Connective Tissue Gene Tests United States1
Institute of Human Genetics Austria1
Institute of Human Genetics India1
Integrated Genetics Westborough United States11
Intergen Genetics and Rare Diseases Diagnosis Center Turkey2
Johns Hopkins Genomics DNA Diagnostic Laboratory United States4
Labcorp Genetics (formerly Invitae) United States26
Lysosomal Diseases Testing Laboratory United States1
Mayo Clinic Laboratories United States5
Molecular Diagnostics Laboratory South Korea1
Molecular Genetics Laboratory Canada1
Molecular Vision Laboratory United States2
Myriad Genetics, Inc. United States1
Natera, Inc. United States11
NxGen MDx United States4
Pittsburgh Cytogenetics Laboratory United States1
Praxis fuer Humangenetik Wien Austria1
Precision Medicine Care (PMC®) United States1
PreventionGenetics, part of Exact Sciences United States21
Quantitative Genomic Medicine Laboratories, SL Spain1
Translational Metabolic Laboratory Netherlands1
Breakthrough Genomics United States0
Dasa Brazil0
Pars Genome Lab Iran0
Victorian Clinical Genetics Services Australia0
Results:
190 genetic tests from 46 labs with tests matching your search, 4 labs matching in other ways
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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

Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel

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

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

NeuromuscularZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
United States
480254
  • 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

Inherited Metabolic Disorders Panel

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

Invitae Skeletal Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
624349
  • D Deletion/duplication analysis

Mitochondrial genome sequencing

Molecular Vision Laboratory
United States
524339
  • 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

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 Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • 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

RenaDx™: Comprehensive Renal Disease Genetics Panel

Precision Medicine Care (PMC®)
United States
470449
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Neuromuscular Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
353208
  • D Deletion/duplication analysis

Invitae Rhabdomyolysis and Metabolic Myopathy Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
202128
  • D Deletion/duplication analysis

Invitae Expanded Renal Disease Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
693388
  • 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
190 tests from 46 labs
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View the list of labs matching your search query.
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❮Page 1 of 10❯
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
Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel by Labcorp Genetics (formerly Invitae), LabCorp
971 conditions, 680 genes
MitoMet®Plus aCGH Analysis by Baylor Genetics
842 conditions, 637 genes
NeuromuscularZoom by Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
480 conditions, 254 genes
Comprehensive Metabolism NGS Panel by Fulgent Genetics
602 conditions, 355 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
Invitae Skeletal Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
624 conditions, 349 genes
Mitochondrial genome sequencing by Molecular Vision Laboratory
524 conditions, 339 genes
Intellectual Disability NGS Panel by Fulgent Genetics
1058 conditions, 554 genes
Beacon Expanded Female Carrier Screening Plus Panel by Fulgent Genetics
716 conditions, 335 genes
Beacon Expanded Female Carrier Screening Panel by Fulgent Genetics
690 conditions, 326 genes
Beacon Expanded Male Carrier Screening Plus Panel by Fulgent Genetics
661 conditions, 306 genes
RenaDx™: Comprehensive Renal Disease Genetics Panel by Precision Medicine Care (PMC®)
470 conditions, 449 genes
Invitae Comprehensive Neuromuscular Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
353 conditions, 208 genes
Invitae Rhabdomyolysis and Metabolic Myopathy Panel by Labcorp Genetics (formerly Invitae), LabCorp
202 conditions, 128 genes
Invitae Expanded Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
693 conditions, 388 genes
qCarrier Plus by Quantitative Genomic Medicine Laboratories, SL
325 conditions, 300 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.