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  • VCV000225368. 29 - ClinVar - NCBI
    Stars represent the aggregate review status, or the level of review supporting the aggregate germline classification for this VCV record This value is calculated by NCBI based on data from submitters Read our rules for calculating the review status The number of submissions which contribute to this review status is shown in parentheses
  • ClinVars Data Model
    ClinVar's Data Model Submitted records Aggregate records Data model infographic Submitted records ClinVar's data model is based on submitted data At a minimum, each submission to ClinVar includes these fields: a variant description a condition the variant is classified for the classification of the variant for the condition at least one observation of the variant; observations may be an
  • VCV000052826. 80 - ClinVar - NCBI
    We've updated the ClinVar website to better support classifications of somatic variants!
  • VCV000012411. 78 - ClinVar - NCBI
    ClinVar contains an entry for this variant (Variation ID: 12411) Based on the evidence outlined above, the variant was classified as uncertain significance Note this variant was found in clinical genetic testing performed by one or more labs who may also submit to ClinVar
  • ClinVar: public archive of interpretations of clinically relevant . . .
    Primary data submissions to ClinVar can help expert groups focus their curation efforts on variants of uncertain significance or those with conflicts in interpretation The resulting interpretations from expert panels as well as from groups that provide practice guidelines may then be submitted to ClinVar
  • VCV000012275. 82 - ClinVar - NCBI
    Search ClinVar Search ClinVar Advanced search About Introduction Data authorities Clinical significance HGVS expressions Submitters Data dictionary Access Access and releases Linking to ClinVar Submit Submission overview Spreadsheets Instructions for spreadsheets Submission Portal FAQ for submissions Assertion criteria Expert panels and
  • VCV000013652. 96 - ClinVar - NCBI
    ClinVar Genomic variation as it relates to human health ClinVar Advanced search About Introduction Data authorities Clinical significance HGVS expressions Submitters Data dictionary





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