How to search ClinVar
Jan 15, 2025 · ClinVar archives and aggregates information about relationships among variation and human health.
Accessing and using data in ClinVar
Jun 4, 2024 · There are multiple ways to identify information in ClinVar on the web. Our help document provides detailed instructions about constructing queries and interpreting the …
ClinVar - National Center for Biotechnology Information
ClinVar archives and aggregates information about relationships among variation and human health.
Submitters - ClinVar - NCBI
ClinVar archives and aggregates information about relationships among variation and human health.
ClinVar: public archive of interpretations of clinically relevant ...
Jan 4, 2016 · The database includes germline and somatic variants of any size, type or genomic location. Interpretations are submitted by clinical testing laboratories, research laboratories, …
ClinVar: public archive of interpretations of clinically relevant ...
The ClinVar database at NCBI archives and aggregates submitted interpretations of the clinical and/or functional significance of variants for specified conditions, with opportunities to provide …
Sources of data in ClinVar
Jan 25, 2024 · ClinVar archives and aggregates information about relationships among variation and human health.
ClinVar: public archive of relationships among sequence variation …
ClinVar (http://www.ncbi.nlm.nih.gov/clinvar/) provides a freely available archive of reports of relationships among medically important variants and phenotypes.
ClinVar at Five Years: Delivering on the Promise - PMC
Launched in 2013 at the National Center for Biotechnology Information, National Institutes of Health, ClinVar is a public database for clinical laboratories, researchers, expert panels, and …
CANVAR: A Tool for Clinical Annotation of Variants Using ClinVar …
ClinVar, a public database, is a central regularly updated repository for variant interpretations submitted by clinical laboratories, researchers, and experts (Landrum et al. 2014; Landrum et …