LogoLogo
  • Getting Started in the VCI and GCI
    • About the Curation Interfaces
    • Account Creation and Login
      • Registration
      • Affiliations
      • Logging In
    • General Navigation
  • VCI Help
    • About Variant Curation
    • Selecting a Variant
    • The Evidence View
    • Starting an Interpretation
      • Interpretation mode view
      • Associating a variant with disease, mode of inheritance and specification document
        • Disease association
        • Mode of inheritance
        • Specification documents
    • Evaluating Criteria
      • Adding Curated Evidence
      • Case/Segregation Data
        • Adding Evidence Details
      • Functional Data
      • The Audit Trail
    • The Evaluation Summary
      • Viewing an Evaluation Summary
        • Modifying a Classification
      • Saving an Evaluation Summary
        • Record Statuses
        • Saving as a Provisional Interpretation
        • Saving as an Approved Interpretation
      • Viewing and Printing Summaries
    • Publishing from the VCI
      • Publishing to the ERepo
      • Publishing to ClinVar
    • Variant Prioritization
      • VP Access
      • Searching
      • The Filter View
      • Filters
      • Columns
      • The VP Data Pipeline
      • Data Output
  • GCI Help
    • About Gene-Disease Clinical Validity Curation
    • Creating a Gene-Disease Record
      • Creating a Free-Text Disease Identifier
    • Curation Central
    • Adding PubMed Articles
      • GCI Preprint Policy
    • Adding ClinVar Submissions
    • Evidence Collection: Overview
    • Evidence Collection: Genetic Evidence
      • Curating Group Information
      • Curating Family Information
      • Curating Individual Information
      • Curating Case-Control Information
      • Curating Variant Information
    • Evidence Collection: Experimental Evidence
      • Biochemical Function Evidence
      • Protein Interactions Evidence
      • Expression Evidence
      • Functional Alteration Evidence
      • Model Systems Evidence
      • Rescue Evidence
    • Previewing Curated Evidence
    • Saving, Reviewing and Approving Classifications
      • Saving the Summary Classification
      • Moving a Gene-Disease Record to Provisional Status
      • Approving a Gene-Disease Record
    • Publishing an Approved Gene-Disease Record
      • Editing the Disease Term of a Published Gene-Disease Record
      • Editing and Re-publishing a Published Summary
    • Recuration
    • GCI API
  • External Tools
    • Ontologies in the VCI and GCI
    • MONDO Search Help
    • HPO Search Help
  • More Information
    • Frequently Asked Questions
    • ClinGen Resources
    • About Us
      • The Team
    • VCI Terms of Use, User Agreement
Powered by GitBook
On this page
Export as PDF
  1. GCI Help

Saving, Reviewing and Approving Classifications

PreviousPreviewing Curated EvidenceNextSaving the Summary Classification

Last updated 2 years ago

Gene-disease curation records move between different states that are indicated by colored labels.

While you are entering evidence, the gene-disease record is shown with an label. When evidence collection is complete and the record is ready for GCEP review, you can save it with a classification label. The Provisional classification will facilitate review of the record by the GCEP by providing summaries of the curated evidence and the associated scores. After the GCEP has discussed the evidence and any requested modifications have been made and saved, the classification can be approved and will then be shown with the classification label.

By saving a Summary or Provisional Classification or approving a classification, you are creating a snapshot of the gene-disease record. You can continue to curate and modify all aspects of the record. However, the snapshot is permanently saved, and its Evidence Summary will be viewable using links in the "Saved Provisional and Approved Classification(s)" section at the bottom of the page when you view the Classification Summary.