Global Genomics Community of 300 000+ healthcare professionals and researchers, who share their findings and expertise and look to establish collaborations. It features a massive knowledge base consisting of 100+ data resources and powerful variant search engine.
VarSome.com Premium is a subscription service allowing you to access additional 3rd party annotation data resources and features without any delays. Free analyses with VarSome Clinical are also included up to the value of your subscription each month.
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.
The latest news from Saphetor SA, the creator of the VarSome Suite.
The latest updates across the whole VarSome Suite.
rs746753722 or CLN6 E227K or NM_017882.3(CLN6):c.679G>A or 15:68500735:A:T
TP53:R175L or NM_000546:R175L or NM_000546(TP53):p.Arg175Leu or TP53:c.524G>T or chr17-7675088-C-A or rs28934578
15-73027478-T-C, X 153418497 A G
chr2:131129929:CTGAAA:, chr13:38320595:GT:, 5:156479558:15:
chr17:37800000:L100000:DUP, chr11:21200000:L90000:DEL, chr7:117138367:117159446:DEL,
chr3:37039445:37059613:DUP, chr21:36160098:36171759:DEL, chr1:110230496:110235917:DUP,
chr21:36160098:36171759:DEL, chr17:43098764:43110978:DEL, chr13:32317656:32331987:DUP,
BRCA1, EGFR, HGNC:1097,
You are in a BETA Environment and any data or results
should not be treated as clinically actionable! If you have any questions, feel free to
Thank you and enjoy your visit!
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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