Genome Variants Explorer
Variant Explorer
Upload a VCF to visualize variants on the GRCh38.p14 reference genome
Drag a VCF file here or click to select
Accepts .vcf and .vcf.gz · Small files: browser-side · Large files: server-side processing
Large file detected
Choose how to load this file:
or try with sample data
or analyze a single variant
FASTQ → VCF Pipeline (coming soon)
FASTQ support requires server-side alignment + variant calling.
For now, run the pipeline locally (e.g. BWA + GATK/Mutect2) and upload the resulting VCF here.
For now, run the pipeline locally (e.g. BWA + GATK/Mutect2) and upload the resulting VCF here.
No data leaves your browser · Reference: GRCh38.p14 · Genome Explorer Phase 2 · More info ↗