VariantTriage — VCF Analysis

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Create a free account to start analyzing variants with AI assistance.

Upload your own VCF files
AI-powered variant interpretation
Filter, sort and export results

Drop VCF files here

or click to browse · .vcf .gz .txt

Zero data transmission. VCF files are processed entirely in your browser — nothing is uploaded, stored, or transmitted to any server. Patient identifiers are automatically removed before display. No genomic or personal data is collected or retained by VariantTriage. In accordance with GDPR data minimisation principles (Art. 5(1)(c)).

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Pathogenic

VUS

Benign

Upload a VCF file to begin

Drag and drop your VCF file into the sidebar, or click to browse. Supports GATK, DeepVariant, Illumina, 23andMe and more.

0 variants

Pri.	Gene	Chr	Position	Ref → Alt	Type	Significance	AF (gnomAD)	Action

Variant Details

Click a variant to see details

AI Assistant

Select a variant to analyze

Generate Clinical Report

PDF report with variant table, AI summaries and clinical notes. Optional fields below.

Clinic / Institution

Sample / Patient ID

Clinician / Analyst

Includes: Summary stats · All 0 filtered variants · Pathogenic highlights · Disclaimer

Export variants

Choose a format — all 0 filtered variants will be exported.

📊

Excel (Windows & Mac)

CSV with semicolons · opens correctly in Excel EU

📄

Standard CSV

Comma-separated · for R, Python, Google Sheets

🔬

TSV (tab-separated)

Standard for bioinformatics tools

Install VariantTriage

Add to home screen for quick access