🚀 October 19, 2026 – PubMind-DB v1.1.1 is now available

A new version of the database is live, covering papers through September 2026. v1.1.1 is now the default for every search type — SNV, genomic variants, gene fusions, CNVs and SVs. v1.0.0 remains selectable for back-tracking.

Variant type	v1.0.0	v1.1.1	Change
SNV	579,844	866,141	+49.4%
Genomic variants (annotated rows)	909,224	1,399,443	+53.9%
Genomic variants (unique alleles)	816,002	1,217,126	+49.2%
Gene fusion	85,966	142,948	+66.3%
CNV	29,457	83,101	+182.1%
SV	69,993	104,310	+49.0%

If you have a PVID from v1.0.0
Searching an old PVID still works — on every variant type. You will either get the same variant, be redirected to its new PVID, or be told it is no longer reported in v1.1.1.

Variant type	Unchanged	Renumbered	Split	Retired
SNV	574,027	5,011	3	803
Gene fusion	85,966	0	0	0
CNV	29,360	0	0	97
SV	69,462	0	0	531

The mapping table lists only the 6,445 identifiers that changed; one that is not in it is unchanged and resolves directly.

Download the v1.0.0 → v1.1.1 PVID mapping table (TSV)

Please cite us at: Wang, P., Wang, K. PubMind: literature-based genetic variant extraction and functional annotation using large language models. Nat Commun 17, 9962 (2026). https://doi.org/10.1038/s41467-026-76834-4

Updated: October 19, 2026