AnyVar
AnyVar enables registration, lookup, and search of genetic variants, as a standalone service or an individual node within a distributed genomic resource network. Its goals are to:
Provide an open source, off-the-shelf solution that lowers the technical barriers for genomic data resources to comprehensively describe and search genomic variants
Support a broad range of query modes, including VRS ID lookups, HGVS expressions, gene-based searches, and genomic ranges
Translate community nomenclatures and conventions into a universal model for variant representation
Provide a community-driven, extensible platform for shared conventions and policy to realize the above goals
If you’re setting up AnyVar for the first time, begin with the Getting Started guide, which covers different installation options. To learn how to use AnyVar programmatically or as a service, see the Usage section. For further assistance, please refer to Getting Help.