Clinical and research tests for GM1 gangliosidosis type 2 - Genetic Testing Registry (GTR) - NCBI

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Condition This summary box displays a gene, condition, or laboratory matching your search query. More help	GM1 gangliosidosis type 2
	Synonyms: GANGLIOSIDOSIS, GENERALIZED GM1, JUVENILE TYPE; GANGLIOSIDOSIS, GENERALIZED GM1, TYPE II; GM1-GANGLIOSIDOSIS, TYPE II; Gangliosidosis, Generalized GM1, Type 2; Juvenile GM>1< gangliosidosis Gene: GLB1

Labs matching your search

25 labs with tests matching your search, 2 labs matching in other ways

Lab name	Tests matching your search
Baylor Genetics United States	1
Bioarray Spain	1
CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	2
CENTOGENE GmbH and LLC - Guiding Precision Medicine Germany	1
CeGaT GmbH Germany	3
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory United States	1
DDC Clinic Molecular Diagnostics Laboratory United States	1
DNA Labs India India	2
Dhiti Omics Technologies Private Ltd India	1
Fulgent Genetics United States	15
GeneDx United States	1
Genetic Services Laboratory United States	2
HNL Genomics Connective Tissue Gene Tests United States	6
Institute of Human Genetics Austria	1
Integrated Genetics Westborough United States	8
Intergen Genetics and Rare Diseases Diagnosis Center Turkey	6
Labcorp Genetics (formerly Invitae) United States	11
Lysosomal Diseases Testing Laboratory United States	2
MNG Laboratories (Medical Neurogenetics, LLC.) United States	1
Mayo Clinic Laboratories United States	2
Myriad Genetics, Inc. United States	1
Natera, Inc. United States	7
Praxis fuer Humangenetik Wien Austria	3
PreventionGenetics, part of Exact Sciences United States	3
Quantitative Genomic Medicine Laboratories, SL Spain	1
Pars Genome Lab Iran	0
Victorian Clinical Genetics Services Australia	0

Results:

83 genetic tests from 25 labs with tests matching your search, 2 labs matching in other ways

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	Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
	Clinical Exome Fulgent Genetics United States	5128	4672	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	CentoNeuro Panel CENTOGENE GmbH and LLC - Guiding Precision Medicine Germany	1886	1858	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	971	680	D Deletion/duplication analysis
	Invitae Skeletal Disorders Panel Labcorp Genetics (formerly Invitae), LabCorp United States	624	349	D Deletion/duplication analysis
	MitoMet®Plus aCGH Analysis Baylor Genetics United States	842	637	D Deletion/duplication analysis
	Beacon Expanded Female Carrier Screening Plus Panel Fulgent Genetics United States	716	335	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Comprehensive Metabolism NGS Panel Fulgent Genetics United States	602	355	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Invitae Cerebral Palsy Spectrum Disorders Panel Labcorp Genetics (formerly Invitae), LabCorp United States	638	419	D Deletion/duplication analysis
	Invitae Comprehensive Deafness Panel Labcorp Genetics (formerly Invitae), LabCorp United States	405	219	D Deletion/duplication analysis
	Epilepsy Comprehensive NGS Panel Fulgent Genetics United States	729	398	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Invitae Comprehensive Neurometabolic Disorders Panel Labcorp Genetics (formerly Invitae), LabCorp United States	351	249	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	qCarrier Plus Quantitative Genomic Medicine Laboratories, SL Spain	325	300	C Sequence analysis of the entire coding region
	Beacon Expanded Female Carrier Screening Panel Fulgent Genetics United States	690	326	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Neonatal Epilepsy NGS Panel Fulgent Genetics United States	509	275	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Comprehensive Epilepsy MNG Laboratories (Medical Neurogenetics, LLC.) United States	414	800	C Sequence analysis of the entire coding region
	Beacon Expanded Male Carrier Screening Panel Fulgent Genetics United States	636	298	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Beacon Expanded Male Carrier Screening Plus Panel Fulgent Genetics United States	661	306	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Inherited Metabolic Disorders Panel Dhiti Omics Technologies Private Ltd India	376	317	C Sequence analysis of the entire coding region
	Invitae Treatable Neurometabolic Disorders Panel Labcorp Genetics (formerly Invitae), LabCorp United States	257	191	D Deletion/duplication analysis C Sequence analysis of the entire coding region
	Non-Immune Hydrops Fetalis Panel PreventionGenetics, part of Exact Sciences United States	292	149	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis

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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.