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VarTracker - Genetic Variant Tracker


cridVarTracker is an online tool for searching multiple public genetic variant databases, displaying genetic variant information merged from a variety of sources. The end-user can search for variants of interest based on a RefSeq ID or Gene, and a cDNA change, and the tool will search and extract data from a variety of public databases, such as ClinVar, NCBI Gene, UniProt, dbSNP, NCBI Books, PubMed, MalaCard, MyVariant, gnomAD, ExAC, Mutalyze and ENSEMBL.






Recent News

Jul 15, 2025 CLIRINX launches the world's most advanced patient-led registry dedicated to Primary Biliary Cholangitis (PBC).

May 1st, 2025 Univ. of Melbourne - Genetic epilepsy study kicks-Off, powered by CLIRINX!

Oct 3, 2024 CRID 'Clinical Research ID' nears 6000 CRID identifiers!

Sep 2, 2024 New Clinical System launched @ Univ. of Melbourne

Jul 1, 2024 The RDDR is now live. https://theRDDR.org

Apr 24, 2024 CLIRINX & CRID feature in new major SCN2A-related publication.