ClinVar archives and aggregates information about relationships among variation and human health. Submission to ClinVar · Sources of data in ClinVar · Using the ClinVar record display

25 јан 2024 · ClinVar is a freely accessible, public archive of reports of human variations classified for diseases and drug responses, with supporting ...

ClinVar is a a freely accessible, public archive of reports of the relationships among human variations and phenotypes hosted by the National Center for ...

Welcome to ClinVar Miner! The content on this website is current as of 3 June 2024. On that date, ClinVar had 4,393,252 submissions on 2,966,675 variants.

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Dərc edildi: 9 мар 2016

ClinVar accessions submissions reporting human variation, interpretations of the relationship of that variation to human health and the evidence supporting each ...

20 ној 2017 · ClinVar (1,2) is a freely available, public archive of human genetic variants and interpretations of their significance to disease. It is ...

ClinVar and ClinGen Partnership · ClinVar is an archival database that aggregates information about genomic variation and its relationship to human health.

ClinVar aggregates information about genomic variation and its relationship to human health. Contact us at 'clinvar@ncbi.nlm.nih.gov' with any questions or ...

13 ијл 2023 · Currently, ClinVar contains just 41 genes in which 10 or more variants are reported as reviewed by an expert panel, out of more than 3000 genes ...