Advance Notice. We are changing the Free API Package for existing users. In order to test and evaluate the VarSome API, anyone interested will be given free access to variants in chromosome 17 only (which contains popular genes BRCA1 and TP53), as...

Since its first launch 3 years ago, VarSome has become a hugely popular platform among clinicians & researchers. We would love to hear from you to understand how you use the platform and how you’d like to see it evolve.

Following feedback from users and advice from our new clinical advisor, we have significantly improved our ACMG classification:

We are proud to release our first complete search feature for VarSome! This 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:

Our team is coming to BioIT World Conference & Expo that takes place in Boston on May 15–17th 2018.

Today we have updated VarSome with a new, clearer layout. We grouped data together by type in a way that hopefully makes it easier to find what you are looking for.

We just added a new component to VarSome: The Structural Variant Browser, a new viewer for structural variants (copy-number and other variants over 100bp in size), from a number of new sources:

We are proud to release a new version of VarSome introducing two new features which we hope you will find useful.

When you scroll down to the Genes section of VarSome, you will see a new colour coded Gene Pathogenicity Matrix. This new feature provides a high-level overview of the spectrum of variants in a single gene and their impact. The data are collated...