Genome → Evidence → Biology → Intelligence
Variant Intelligence
Search a human variant by rsID, HGVS identifier or gene. NuCell resolves it across ClinVar submitter records, Ensembl transcript consequences, gnomAD frequency, AlphaMissense, CPIC pharmacogenomics and literature — then reasons over that evidence, with every claim traceable to its source.
Try
Whole genome
Drop a VCF or VCF.GZ to analyse a whole genome
The file is read inside your browser and never uploaded. NuCell ranks its variants by predicted consequence, rarity and ClinVar signal, then looks up evidence only for the variants you choose to open.