Global Genomics Community of 250'000+ healthcare professionals and researchers, who share their findings and expertise and look to establish collaborations. It features a massive knowledge base consisting of 70+ data resources and powerful variant search engine.
CE IVD-certified and HIPAA-compliant platform for variant discovery, annotation, and interpretation of NGS data for whole genomes, exomes, and gene panels, for individual samples, trios, families, and cohorts.
All our platforms provide powerful programming interfaces which allow you easy integration with your own software tools.
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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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