Upload your VCF file and get a clear, structured overview of genetic variants with priority indicators and human-readable explanations.
| Gene | Position | Type | Priority | Note |
|---|---|---|---|---|
| RPGR | chrX:38,152,229 | Missense | High | Known pathogenic variant |
| RHO | chr3:14,182,883 | Missense | High | Likely pathogenic |
| USH2A | chr1:216,595,579 | Splice site | Medium | Variant of interest, VUS |
| PRPF31 | chr19:17,942,600 | Synonymous | Low | Likely benign |
| TULP1 | chr6:35,517,208 | Intronic | Low | Benign, no known effect |
— Features
Load any standard VCF file — GATK, DeepVariant, Illumina, 23andMe — and get structured results in seconds.
Variants are automatically triaged into High, Medium, and Low tiers. You always know where to look first.
No cryptic annotations. Each variant ships with a plain explanation and direct links to ClinVar and OMIM.
All analysis runs on your machine. No internet required for core features. Your files never leave your device.
Chromosome maps, severity breakdowns, gene frequency charts — rendered instantly without external tools.
Export clean PDF reports or CSV tables. Share with colleagues or keep as structured documentation.
— Workflow
Four steps. Under sixty seconds. No configuration required.
— Changelog
Every release, documented. We ship improvements every few weeks.
— Comparison
See how we compare to typical alternatives for variant review workflows.
| Feature | VariantTriage | IGV / Generic viewers | Cloud-based tools |
|---|---|---|---|
| Instant priority triage | ✓ | ✗ | Partial |
| 100% local processing | ✓ | ✓ | ✗ |
| Human-readable explanations | ✓ | ✗ | Partial |
| No setup / no CLI required | ✓ | ✗ | ✓ |
| PDF & CSV export | ✓ | Partial | ✓ |
| No subscription fee | ✓ | ✓ | ✗ |
| Works in any browser | ✓ | ✓ | ✗ |
— Why VariantTriage
Open your browser and start analyzing. No installation, no configuration, no command line required.
Your VCF files are processed entirely on your local machine. Nothing is ever transmitted to any server.
Works completely offline for all core analysis. ClinVar lookups are optional and clearly indicated when used.
From raw VCF to prioritized, readable output in under 60 seconds. No queue, no wait, no friction.
— Pricing
No subscriptions. No recurring fees. Pay once, use forever on any machine.
Try the app with demo data. No account needed.
Full access for individual researchers, clinicians and analysts.
For clinical labs, research groups and small teams.
— FAQ
Everything you need to know about VariantTriage.
— Get started today
Join researchers worldwide who use VariantTriage to work through variant data faster and with more clarity.