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. VCI Help
  2. The Evaluation Summary

Viewing and Printing Summaries

PreviousSaving as an Approved InterpretationNextPublishing from the VCI

Last updated 2 years ago

How to View Summaries

Upon saving all Provisional and Approved Interpretations a snapshot of their Evaluation Summary is also saved. A Summary is viewable for each Interpretation from the "Saved Provisional and Approved Interpretation(s)" on the Evaluation Summary page by clicking on the "View Provisional Summary" and "View Approved Summary" buttons. For archived Interpretations these buttons appear gray but they are still active linkouts to the Summaries.

Summaries

A Summary snapshot will contain a Summary table at the top with information about the Interpretation, followed below by the Evidence Summary, and finally the criteria tables underneath.

Printing Summaries

Recommended print settings:

  • Layout: Landscape

  • Scale: 50%

  • Margins: Minimum

  • Background graphics selected

You can also use your Print dialogue box to save your Interpretation as a PDF.

You can print an Interpretation Summary by using the button in the footer following the criteria tables.