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.
Examples (1)
Default ClinVar Get Submitted Records call
Anonymous-safe example. Rate-limited; no sign-in required.
Identifiers
- Catalog ID
- tu_ClinVar_get_submitted_records
- Tool name
- ClinVar_get_submitted_records
- Added
- 2026-07-29 18:13Z
- Tags
- tooluniverse