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Many people visit NCBI’s ClinVar site every day, multiple times a day. As the field of clinical genetics advances, more and more new visitors also come to ClinVar to research the clinical significance of genetic variants. Based on feedback from new and existing customers, we are improving the homepage to serve as a better introduction to data and services within the resource.
What’s new?
Improved ClinVar homepage:
The new ClinVar homepage will allow users to become familiar with the ClinVar data model – how we store and aggregate the data provided by submitters – as well as the organizations that submit data to ClinVar. Visitors can also browse the various methods used to access data in ClinVar.
Updated menu structure:
From the homepage, you will still be able start a new search and go to individual variant pages as before. An updated menu structure will allow you to find more information about ClinVar quickly.
ClinVar’s new design will be geared towards quick summary views and will be mobile friendly!
Stay up to date
Connect with NLM on social media and join our mailing list to stay up to date on ClinVar.
We want to hear from you!
Please write to us with any feedback or questions at [email protected].
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