VarTracker - Genetic Variant Tracker
VarTracker 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
Sep 1, 2026 Inchstone/DEE-P launches major 'Parents Speak' research study using CLIRINX
Jun 1, 2026 CRID reaches 10,000 identifiers.
Mar 1, 2026 CLIRINX selected for Parents Speak/Inchstone Project study.
Feb 1, 2026 First paper published for CLIRINX platform from the PBC Ireland Patient Registry.
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.