One platform for clinical genomics
interpretation and reporting.
Vgen23 brings evidence review, ACMG classification, variant prioritization, and reporting into a single environment for germline and somatic workflows.
Stop switching between tools.
Vgen23 brings the core interpretation workflow into one workspace so genetics teams can review evidence, classify variants, and move cases into report-ready drafts without juggling multiple tabs and manual report assembly.
Review each variant with annotation from 100+ databases, including ClinVar, gnomAD, OMIM, PubMed, and Indian Genome allele frequency data.
Apply ACMG/AMP criteria with a visible evidence trail, editable logic, and audit-logged review.
Pull structured literature and disease relevance into the case review flow with citations.
Convert referral-note language into standardized HPO terms without manual lookup.
Inspect alignment and variant support inside the same case workspace.
Visualize relationships between variants, genes, diseases, and phenotypes across a case.
Select variants and move them into report-ready drafts with supporting context already in place.
Built for reviewability
Vgen23 is designed to help teams review faster without losing traceability. Evidence stays visible. Changes stay logged. Final outputs stay ready for professional review and sign-off.
Explore WorkflowsBuilt for real lab workflows
Whether your team works on rare disease exomes, family-based analysis, targeted panels, or somatic interpretation, Vgen23 keeps the workflow structured from upload to report-ready draft.
2 minutes to create an account. Instant access.