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ncbi-variation

pipeworx.ioInfrastructure

No liveness check has reached it yet; it has been in the index since 10 Oct 2026. How this is checked

Ncbi Variation is a Pipeworx-hosted MCP server exposing tools for NCBI Variation Services. It retrieves dbSNP refSNP records, normalizes HGVS expressions to SPDI, and maps SPDI alleles to dbSNP rsIDs for genomics workflows.

Inferred · not functionally tested

WebAPICloud-managed
ncbi-variation preview
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Overview

6 features

Purpose: Querying authoritative dbSNP variant records and converting between HGVS, SPDI, and rsID representations.

Inferred · not functionally tested

Audience: genomics researchers, clinicians, and bioinformatics developers

Inferred · not functionally tested

Functions: data_extraction

Inferred · not functionally tested

Interfaces: API: indicated (inferred, not tested) · MCP: indicated (inferred, not tested) · CLI: unknown · Self-hosting: unknown

Recorded constraints: pricing: unknown · license: Proprietary · platforms: WEB · deployment: browser, api_only, cloud_managed

Constraint provenance is unknown; confirm requirements with the publisher.

Record sources: gateway.pipeworx.io. These links do not verify the individual claims.

ncbi-variation sits in PulseGate's API design, testing & docs category. Inferred · not functionally tested: It focuses on querying authoritative dbSNP variant records and converting between HGVS, SPDI, and rsID representations. Inferred · not functionally tested: It is built as a B2B product for genomics researchers, clinicians, and bioinformatics developers. Basis unknown · not verified: It runs on the web and API.

Pipeworx builds and maintains ncbi-variation. Inferred · not functionally tested: Among its 6 catalogued features are dbSNP lookup, HGVS normalization, and SPDI conversion. Inferred · not functionally tested: Catalogued interfaces include an MCP server and a public API.

Summary written by a language model from the project’s public pages.

Tasks: Inferred · not functionally tested

  • dbSNP lookup
  • HGVS normalization
  • SPDI conversion
  • rsID mapping
  • Genomic coordinates
  • HGVS expressions

Topics: Inferred · not functionally tested

Tags
ncbi-variationdbsnpvariant-normalizationgenomics-api

JSON profile · Text profile · Access guide

Built with & integrations

Hosting
Cloudflare
Connectors
MCPAPI
Runs on
BrowserAPI-onlyCloud-managed
Detected from
Cloudflare
cf-ray header

Trust & compliance

Public signals
HTTPS

Indexing history

1

What PulseGate has recorded for this listing

  1. Indexed10 Oct · 00:02 UTC
    Ncbi Variation seen via MCP Registry (official)
    Source: MCP Registry (official) · Open

Frequently asked questions about ncbi-variation

What does ncbi-variation do?
Inferred · not functionally tested: Ncbi-variation focuses on querying authoritative dbSNP variant records and converting between HGVS, SPDI, and rsID representations. It is catalogued under API design, testing & docs on PulseGate.
Who is ncbi-variation for?
Inferred · not functionally tested: ncbi-variation is a B2B product built for genomics researchers, clinicians, and bioinformatics developers.
What platforms does ncbi-variation run on?
Basis unknown · not verified: ncbi-variation runs on the web and API.
Is ncbi-variation still maintained?
Unverified. ncbi-variation has not been re-checked since it entered the index, so there is no finding either way — and only a positive finding would say otherwise.
Who makes ncbi-variation?
ncbi-variation is developed by Pipeworx.
Does ncbi-variation have an API or integrations?
Inferred · not functionally tested: Yes — ncbi-variation exposes an MCP server and a public API.

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