Clinical and research tests for 1471 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
CST3 Gene Cerebral amyloid angiopathy NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning of the entire coding region
Cerebrovascular Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	23	30	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CentoNeuro Panel Centogene AG - the Rare Disease Company Germany	1886	1858	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel PreventionGenetics, part of Exact Sciences United States	346	160	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Invitae Hereditary Cerebral Small Vessel Disease Panel Labcorp Genetics (formerly Invitae) LabCorp United States	24	10	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cerebral amyloid angiopathy, 105150, Autosomal dominant (Hereditary cerebral hemorrhage with amyloidosis) (CST3 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Macular degeneration, age-related, 11, 611953; ARMD11 (Hereditary cerebral hemorrhage with amyloidosis) (CST3 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Hereditary Lymphoid/Immunodeficiency Predisposition Panel Genetic Services Laboratory University of Chicago United States	27	66	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Neurodegenerative panel _v.2.0 CGC Genetics Unilabs Portugal	15	207	C Sequence analysis of the entire coding region
Hereditary amyloidosis (WES based NGS panel of 21 genes, including CNV analysis) CGC Genetics Unilabs Portugal	1	21	C Sequence analysis of the entire coding region
Cerebral small vessel disease panel CGC Genetics Unilabs Portugal	1	18	C Sequence analysis of the entire coding region
Macular Degeneration Panel CGC Genetics Unilabs Portugal	1	20	C Sequence analysis of the entire coding region
Cerebral amyloid angiopathy (sequence analysis of CST3 gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
STARGARDT DISEASE EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	49	E Sequence analysis of select exons
DEMENTIA AND ALZHEIMER EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	68	E Sequence analysis of select exons
ALZHEIMER AND DEMENTIA EXOME PANEL Laboratorio de Genetica Clinica SL Spain	1	68	E Sequence analysis of select exons
HEREDITARY AMYLOIDOSIS SYNDROME PANEL Laboratorio de Genetica Clinica SL Spain	1	22	E Sequence analysis of select exons
Familial Amyloidosis Genologica Medica Spain	44	19	C Sequence analysis of the entire coding region
Cerebral amyloid angiopathy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	3	3	C Sequence analysis of the entire coding region
Cerebral amyloid angiopathy, CST3-Related Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Germany	1	1	C Sequence analysis of the entire coding region

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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.