ClinVar
ClinVar aggregates information about genomic variation and its relationship to human health.
What's in ClinVar?
In this section
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How ClinVar Models its Data
Learn how ClinVar aggregates multiple submissions for a variant in one VCV record and how these submissions can also be viewed by condition in RCV records.
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List of ClinVar Submitters
ClinVar is built from data that is voluntarily shared by organizations around the world. Get to know our community.
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Ways to Access Data
ClinVar data can be viewed on the website, downloaded by FTP, and accessed programmatically by API. Find the best way to get to the data you need.
World-wide Participation in ClinVar
| Submitters Per Country | |||||
| 300+ | 100-299 | 50-99 | 10-49 | 1-9 | None |
Submission to ClinVar
ClinVar welcomes submissions from clinical testing labs, research labs, genetics clinics, patient registries, locus-specific databases, expert panels, and groups establishing practice guidelines.
Submission PortalIn this section
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New to Submission
Get an overview of how submission to ClinVar works and learn what the benefits are.
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Ready to Get Started?
Register your organization, get familiar with the ClinVar submission process, and select a submission method that fits your needs.
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How to Prepare Your Submission Data
Learn how to prepare and submit your data.
The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. NIH does not independently verify the submitted information. If you have questions about the information contained on this website, please see a health care professional. More information about NCBI's disclaimer policy is available.
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