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NCBI ClinVar Variant Data Export

Data Export of NCBI ClinVar Variant. Structured, ready-to-use data exported in seconds for research, monitoring, or lead generation.

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NCBI ClinVar Variant Scraper
NCBI ClinVar Variant Scraperparseforge/clinvar-esummary-scraper
accession
title
clinical_significance
gene
+8 fields
Text
Number
Boolean
List
Object

Input

Maximum records:100
Gene or variant term:BRCA1

Output fields

accession
title
clinical_significance
gene
condition
review_status
last_evaluated
variation_type
hgvs
submitters
scrapedAt
error

How it works

Sign up on Apify or log in

The NCBI ClinVar Variant Scraper Actor is ready to run with the inputs already set for "NCBI ClinVar Variant Data Export". Sign up or log in and you'll land in Apify Console with a copy of this exact task.

Start the "NCBI ClinVar Variant Data Export" task

The NCBI ClinVar Variant Scraper Actor will start running based on the input automatically. You can also change all the input fields, like maximum records and gene or variant term, to match your specific use case.

Receive the "NCBI ClinVar Variant Data Export" output

Monitor the progress in real time. You will be notified as soon as your dataset is complete and ready for review. Each result includes data such as accession, title, clinical_significance, and more.

Integrate into your workflow

The final output is delivered in JSON, CSV, or Excel format, ready to be plugged into your workflow. You can also run the "NCBI ClinVar Variant Data Export" task via API.

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Integrate "NCBI ClinVar Variant Data Export" into your workflow

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