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VarSome: NGS Data Analysis

Search engine for the human genomic variant

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VarSome: A search engine for the human genome.

Three different levels for communities, researchers, and clinicians.

VarSome.com

A community-driven project to share global expertise on the human genome.

Over 300,000 users worldwide.

Join the community at VarSome.com

VarSome Pemium

A subscription-based service for researchers and clinicians. With a premium subscription, you have access to annotation data, additional resources, and features.

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VarSome Clinical

A HIPPA-compliant and CE IVD-certified platform offering fast and accurate variant discovery, interpretation, and annotation of NGS data.

Schedule your free consultation today

VarSome API

You can annotate variants with data from more than 80 genomic databases. Start your project quickly with our simple API.

Learn more about the VarSome API
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We Use Data to Improve Patient Outcomes

1Faster, more accurate diagnoses to help clinicians find the best therapies.

2Consistent, accurate data, for better outcomes.

3Save time and effort with cutting-edge tools and platforms.

Large-scale analysis of NGS data

Saphetor is pioneering, genome-scale annotation, analysis, and interpretation of
NGS data for better clinical outcomes.

© 2021 Saphetor SA – All Rights Reserved.