VarSome is a community-driven project for sharing global expertise on human variants. Our cross-referenced knowledge base integrates more than 140 genomic data sources, with input from over …

VarSome’s powerful knowledge base is supported by our expert variant curation team and a global community of over 500 000 clinicians, researchers, and bioinformaticians in over 150 countries, …

VarSome is home to a leading genomics interpretation community - a global community of users who contribute knowledge, share variant data, and access curated resources every day.

Our complete search feature expands the existing search functionality of VarSome, enabling you to search not only for variants, but also to perform word searches over the entire contents of VarSome: …

VarSome's high-performance API enables variant annotation from over 140 integrated databases. Start your project immediately, without incurring the significant overheads of multiple integrations and …

Search for anything in the VarSome database. Examples: macular degeneration, "royal disease", article fish eye. More information... Formats accepted for variant, gene, transcript, position and region …

VarSome brings together data, technology, and a global community to advance genomic interpretation. The platform integrates more than 140 curated databases, including ClinVar, gnomAD, OncoKB™, …

Oct 30, 2018 · VarSome is both a powerful annotation tool and search engine for human genomic variants, and a platform enabling the sharing of knowledge on specific variants. Since its initial …

VarSome provides interactive genome and region browsers to explore SV breakpoints and their affected regions. Users can examine gene disruptions, overlaps with regulatory regions, and supporting …

Oct 17, 2025 · VarSome runs best on recent versions of Chrome, MS Edge, Firefox and Safari on Windows, MacOS, Linux, Andriod and iOS. Please make sure you regularly update your browser.