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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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  1. Getting Started in the VCI and GCI
  2. Account Creation and Login

Registration

PreviousAccount Creation and LoginNextAffiliations

Last updated 9 months ago

When to Register

We recommend curators become familiar with the interface by exploring the test interface before curating “real” evidence into the production interface.

How to Register

We have two sites, the production site at and the test site at .

Each site requires its own registration (i.e. registering for one site does not create an account for the other).

The email address you register with will be your username.

Username and Password are both case-sensitive.

This means that if you register as "User@email.com", you will NOT be able to log in as "user@email.com" or as "USER@EMAIL.COM"

To register for either site:

Click Login in the upper right corner.

Click Create Account in the sign-in screen.

Fill out the form and click Create Account to submit the request.

  • The test site will automatically add you as a curator.

Retrieve the code from your email and use that to authenticate your email address. You will also be asked to agree to the site's .

For the production site you must be validated by an admin to finalize access. This may take a few days and you will be emailed when it's completed. Email us at to expedite the process.

If you are a part of a curation affiliation, please follow the above steps and also ask your coordinator to arrange for you to be added to the affiliation. The ClinGen Variant Curation Interface is available for public use. The ClinGen Gene Curation Interface is restricted to use by ClinGen curators. If you would like to collaborate on gene curation, please contact ClinGen at .

Terms of Use
clingen-helpdesk@lists.stanford.edu
clingen@clinicalgenome.org
https://curation.clinicalgenome.org/
https://curation-test.clinicalgenome.org/