ClinVar

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.

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.

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.

About the ClinGen and ClinVar Partnership

Learn more about ClinVar and ClinGen's partnership to improve our knowledge of clinically relevant genomic variation.

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ClinVar Submission

ClinVar provides detailed instructions on submitting data. We recommend that you first review the ClinVar Submission Overview page to familiarize yourself with the submission process and submission template. We also providean overview of the ClinVar submission instructions adapted by ClinGen.

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