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  • 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
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  • Landing Page
  • Dashboard View
  • Begin Curation
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  1. Getting Started in the VCI and GCI

General Navigation

PreviousLogging InNextAbout Variant Curation

Last updated 2 years ago

Landing Page

When you first login, you will be on the landing page, which contains general information about ClinGen and the VCI and GCI. To access your curations, head to the dashboard.

Dashboard View

Navigation Bar

Available from all pages. From here you can:

Affiliation Bar

On the Test site, all users can select "Test Site Example Affiliation" to access the GCI

Header

Displays the account and affiliation you are logged in under.

Tool Bar

To select which curation table(s) to display on the dashboard.

My ClinVar Submission Batches - This displays both current and closed ClinVar submission batches for the selected affiliation. Note: This option only appears when logged into an affiliation.

Curation Tables

  • By default, the dashboard will open to My Variant and Gene Interpretations.

  • All tables have similar functionality. Users can:

    • Search/filter on any text in any text field

    • Download the table as a .csv file

    • Navigate with pagination features and expand the number of curations displayed at once (up to 100)

  • The My Variant Interpretations and My Gene-Disease Records tables have additional detail and functionality.

    • Columns for status, classification, met criteria (variant only), and date last modified

    • Ability to filter by status (In Progress, Provisional, Approved and Published)

Search tips:

Not case-sensitive

No wild cards search features

Total count updates and table rows filter as you type

Begin Curation

For assistance with the VCI, click Next, or go to:

For assistance with the GCI, go to:

Access the variant prioritization tool

Initiate a new variant curation

Initiate a new gene curation; disabled (grayed out) if not logged in to a ClinGen GCEP affiliation

Return to the dashboard

Access help resources. Pulldown menu options include links to this documentation, GCI and VCI SOPs, Terms of Use/User Agreement, GeneTracker tool (requires separate login), and email helpdesk.

Log out of the interface

Available from all pages. Displays current affiliation. Click to change the affiliation you are curating under.

All Variant Interpretations – This list contains all Interpretations curated to date, by all users/affiliations, along with disease/mode of inheritance, and date created.

My Variant and Gene Interpretations - These tables list all VCI and GCI entries for the user or logged-in affiliation.

All Gene-Disease Records – This list contains all the Gene-Disease Records curated to date, by all users/affiliations, along with disease/mode of inheritance, and date created.

VCI Help
GCI Help
Default Dashboard View with My Interpretations Tables
All Variant Interpretations Table
All Gene-Disease Records Table