VarSome is a global community of experts sharing their knowledge of human variants. Leverage VarSome’s comprehensive knowledge base, variant search engine, ACMG annotation and community contributions to empower your own work.
Need to analyze gene panels, exomes or whole genomes? VarSome Clinical is our clinically-certified platform, covering all aspects of variant discovery, annotation, interpretation, and reporting. It is used daily by professionals in leading hospitals and laboratories worldwide.
We provide a powerful programming interface that allows you to quickly integrate the full power of VarSome into your own bioinformatics pipeline, hugely reducing your time to market, development, and data maintenance costs.
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With VarSome Pro you can upload a VCF file containing simple or multiple samples for variant annotation and classification. Subsequently, you can use a sophisticated set of features for browsing and filtering your data.
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