Enter a variant and read what the public registries hold about it, every assertion linked to the record it came from. VarInsight adds no interpretation of its own.
What this accepts — 8 formats, each example runs when clicked
- rsID
- VCF-style coordinate
- or
- Genomic HGVS
- or
- Coding or protein HGVS
- or
- Gene and change
- or
- ClinVar Variation ID
- ClinVar’s own identifier, pasted as it stands
- Ensembl or LRG notation — resolved by Ensembl, which is slow
- or
Enter a variant, or click any example above to run it.