Store and access millions of variants efficiently with a robust architecture built for high-throughput genomics.
Get instant calculations of allele frequencies, heterozygosity rates, and other critical metrics specific to your population dataset.
Access annotations from leading databases, search using flexible filters, and locate all samples containing a specific variant — all through an intuitive UI.
Import data using VCF, TSV, CSV, and custom formats. VariantBase ensures seamless compliance with HGVS nomenclature standards.
Leverage built-in semantic search to connect phenotypes and diseases using popular ontologies like HPO — even for non-experts.
Connect effortlessly to your Hospital Information Systems (HIS), EMRs, or third-party variant analysis tools. Automate data flows and accelerate your interpretation pipelines.
Tailored to meet the needs of professionals at every stage of the genomic pipeline.
For internal collaboration and variant reclassification
To interpret variants for precision medicine
To identify novel pathogenic or population-specific variants
Store and access millions of variants efficiently with a robust architecture built for high-throughput genomics.
Get instant calculations of allele frequencies, heterozygosity rates, and other critical metrics specific to your population dataset.
Access annotations from leading databases, search using flexible filters, and locate all samples containing a specific variant — all through an intuitive UI.
Import data using VCF, TSV, CSV, and custom formats. VariantBase ensures seamless compliance with HGVS nomenclature standards.
Leverage built-in semantic search to connect phenotypes and diseases using popular ontologies like HPO — even for non-experts.
Connect effortlessly to your Hospital Information Systems (HIS), EMRs, or third-party variant analysis tools. Automate data flows and accelerate your interpretation pipelines.
Unlock the full potential of your in-house genetic data with a platform built for collaboration, accuracy, and scale.
Break down barriers across departments and unify access to variant information for all teams.
Improve curation accuracy with seamless collaboration between clinicians, counselors, and researchers.
Prioritize genetic variants with insights tailored to your specific patient population.
Minimize manual effort through automation, flexible imports, and smart variant updates.
Scale confidently with a modern, AI-enabled platform designed for tomorrow’s genomic needs.
VariantBase is not just another variant database — it's your private, decentralized knowledge hub, capturing variants identified from your patient samples and enriched with comprehensive annotations and metrics.
Build a private internal network for your molecular lab teams. Share insights, annotate rare variants, and align on reclassifications — all within a secure, role-based collaboration space.
Support your variant interpretation workflows with built-in ACMG/AMP reclassification tools, phenotype-aware AI-assisted search, and seamless integration with third-party platforms like Golden Helix VarSeq.
VariantBase empowers your lab to lead in precision medicine by giving you total control over your variant data, insights, and decisions — without relying on external databases that don't reflect your unique population.
Join the growing number of clinical and research labs that trust VariantBase to power their genomic insights.