ClinVar Get Submitted Records
Retrieve the individual per-submitter assertions (SCV / ClinicalAssertion records) for a ClinVar variant. Unlike ClinVar_search_variants / ClinVar_get_variant_details / ClinVar_get_clinical_significance (which use esummary and return only the single AGGREGATE germline classification), this tool calls NCBI eutils efetch (rettype=vcv) and parses the full VariationArchive XML to expose every submitter's own classification, review status, condition and last-evaluated date. Use this when you need to…
Overview
Retrieve the individual per-submitter assertions (SCV / ClinicalAssertion records) for a ClinVar variant. Unlike ClinVar_search_variants / ClinVar_get_variant_details / ClinVar_get_clinical_significance (which use esummary and return only the single AGGREGATE germline classification), this tool calls NCBI eutils efetch (rettype=vcv) and parses the full VariationArchive XML to expose every submitter's own classification, review status, condition and last-evaluated date. Use this when you need to see who classified a variant and how (e.g. to inspect conflicting interpretations behind a 'Conflicting classifications of pathogenicity' aggregate). Keyless NCBI endpoint.
Schema
JSON Schema the agent (or your API call) must match.
View JSON schemaExpandCollapse
Examples (1)
Default ClinVar Get Submitted Records call
Public-safe example · rate-limited
Identifiers
- Catalog ID
- tu_ClinVar_get_submitted_records
- Tool name
- ClinVar_get_submitted_records
- Added
- 2026-07-29 18:13Z
- Tags
- tooluniverse