ClinVar archives and aggregates information about relationships among variation and human health. Submission to ClinVar · The ClinVar variation report · Advanced · About

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 ...

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

28 ној 2019 · ClinVar is a freely available, public archive of human genetic variants and interpretations of their relationships to diseases and other ...

Welcome to ClinVar Miner! The content on this website is current as of 2 May 2024. On that date, ClinVar had 4,385,716 submissions on 2,963,045 variants.

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 ...

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

Boolean operators allow you to combine search terms: AND: Finds documents that contain both terms. OR: Finds documents that contain either term.

Abstract. ClinVar (http://www.ncbi.nlm.nih.gov/clinvar/) provides a freely available archive of reports of relationships among medically important variants.