ClinVar is a a freely accessible, public archive of reports of the relationships among human variations and phenotypes hosted by the National Center for Biotechnology Information (NCBI) and funded by intramural National Institutes of Health (NIH) funding. ClinGen investigators work closely with NCBI regarding the development and functionality of ClinVar and to support data deposition from many sources; ClinGen curation efforts will constantly improve the data within ClinVar.
Visit the ClinVar site today to search for information on genomic variants! Not sure how to use ClinVar? Check out the links below for selected "how-to" resources from the ClinVar team. Always check the ClinVar site for the most up-to-date information regarding resource utilization. For instructions and guidance on submitting to ClinVar, visit the ClinVar Submission page and ClinGen's Data Sharing Guidance page.
ClinGen Community ClinVar Call
Beginning in January 2016, the ClinGen Community ClinVar call on the 4th Friday of each month will bring together members of ClinGen and any interested user of ClinVar to suggest and discuss topics about using or submitting to ClinVar. If you would like to join the mailing list to receive call information and a monthly reminder please email us. If you have a topic you would like to add to the agenda, please use our topic request form.