lab
For the lab

Full-fidelity variant data.

Query, filter, export — every row, every annotation. The complete InterVar/ACMG picture with nothing collapsed away.

Compare experiences
› filter clinvar=Pathogenic cadd>20 --export tsv
genehgvsclinvarCADD
SERPINA1c.863A>TPathogenic29.4
PADI3c.881C>TPathogenic26.1
PAX6c.112C>TPathogenic24.8
No detail dropped

Query everything

The full report, indexed — not a summary.

Compose any filter

ClinVar, InterVar, ACMG flags, CADD, gnomAD, zygosity, region — stack predicates over all 76k+ rows.

Full annotation set

Nothing collapsed. Every column from the InterVar/ANNOVAR export is queryable and visible.

Export what you find

Pull any result set to TSV for your own pipeline — reproducible, row-accurate.

Whole-genome scale

10k–100k+ variants per report, indexed for sub-second deterministic queries.

Sample queries

Ask in the language you think in

Returns the ClinVar-Pathogenic rows above the CADD threshold with full HGVS, zygosity and population frequencies — sourced verbatim from the parsed rows.
Trust the numbers

Deterministic by construction

The model renders prose; the counts and rows come from code.

Counts are computed

Aggregates run over parsed rows in Python — never hallucinated. A validator strips anything off-report.

Row-traceable

Every value carries its source row, so any figure can be reproduced against the raw file.

Open the lab console

Filter, inspect and export your report's full variant set.