Interactive Demo — Baseshift Variant Analysis in 60 Seconds

Choose analysis type

Baseshift supports targeted panels, exome sequencing, and whole genome. Pricing and file limits adapt automatically.

🔬 Targeted / Exome

Panel VCFs, exome capture. Up to 250 MB per file.

$15 / sample

🧬 Whole Genome

WGS VCFs, full chromosomal coverage. Up to 10 GB per file.

$40 / sample

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Drop your VCF file here

Or click to browse — .vcf and .vcf.gz files supported

sample-data.vcf

⬇ Download sample VCF

Analysing variants…

Baseshift parses your VCF, looks up each variant in ClinVar and gnomAD, then asks an AI model to classify pathogenicity and write a clinical annotation. This takes ~2 minutes on a real file.

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Parsing VCF

Reading chromosomal positions, alleles, quality scores

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ClinVar lookup

Matching variants against clinical significance database

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gnomAD frequency

Population allele frequencies from gnomAD v4 (126,756 genomes)

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AI annotation

Pathogenicity classification, HGVS notation, clinical summary

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Generating clinical report

PDF with variant table, statistics, and interpretive summary

Estimating time…

Analysis Complete

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Chr	Position	Alleles	HGVS	Gene	Zygosity	Pathogenicity	Impact	gnomAD	Annotation

Top Genes

Chromosomes

Variant Types

Impact Scores

Clinical PDF report

Baseshift generates a downloadable PDF with variant table, statistics, and a full clinical interpretive summary — ready to share with your team.

baseshift

Genomic Variant Analysis Report

Sample

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Total Variants

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Annotated

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Analysis Date

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▲ Priority Variants

Ready to analyze your own data?

Your first sample is free

Create an account and upload your VCF — Baseshift runs the full AI annotation pipeline and generates your clinical report in under 2 minutes.

Start free analysis → View full sample report

First sample free $15 / exome · $40 / WGS Results in ~2 minutes No subscription

See your first variant report in 60 seconds

🔬 Targeted / Exome

🧬 Whole Genome

Drop your VCF file here

Your first sample is free