appears_in: []
depends_on: []
deprecated: false
description: ClinVar archives reports of relationships among medically important variants
  and phenotypes. It records human variation, interpretations of the relationship
  specific variations to human health, and supporting evidence for each interpretation.
  Each ClinVar record (RCV identifier) represents an aggregated view of interpretations
  of the same variation and condition from one or more submitters. Submissions for
  individual variation/phenotype combinations (SCV identifier) are also collected
  and made available separately. This collection references submissions, and is based
  on SCV accession.
example: SCV000151292
example_extras: []
homepage: http://www.ncbi.nlm.nih.gov/clinvar/
keywords: []
mappings:
  biocontext: CLINVAR.SUBMISSION
  miriam: clinvar.submission
  n2t: clinvar.submission
name: ClinVar Submission
namespace_in_lui: false
owners:
- name: National Center for Biotechnology Information
  ror: 02meqm098
pattern: ^SCV\d+(\.\d+)?$
preferred_prefix: clinvar.submission
prefix: clinvar.submission
providers: []
publications: []
synonyms: []
uri_format: http://www.ncbi.nlm.nih.gov/clinvar?term=$1
