NCBI ClinVar Variants Scraper
by parseforge
Scrapes NCBI ClinVar for genetic variant records by gene, condition, or free-text query. It runs on Apify at $0.0210/result and has 2 users.
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TL;DR: NCBI ClinVar Variants Scraper by parseforge is built for news & content workflows. It has 2 users and runs on $0.0210/result.
What It Does
Scrapes NCBI ClinVar for genetic variant records by gene, condition, or free-text query. Returns each variant as a flat row with clinical significance, review status, and associated conditions.
Key Stats
- Users
- 2
- Total Runs
- 99
- Pricing
- $0.0210/result
- Rating
- View on Apify →
Quick Answers
Teams that need a ready-made news & content actor and want to compare pricing, reviews, and actor activity before running it.
Test a small run first, export the sample output, then decide whether the pricing model works for your volume.
parseforge/ncbi-clinvar-variants-scraper
$0.0210/result
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Read guide →Common Questions
What is NCBI ClinVar Variants Scraper?
Scrapes NCBI ClinVar for genetic variant records by gene, condition, or free-text query. Returns each variant as a flat row with clinical significance, review status, and associated conditions.
How much does NCBI ClinVar Variants Scraper cost?
NCBI ClinVar Variants Scraper costs $0.0210/result on Apify, and the free tier lets you test it before upgrading.
Is NCBI ClinVar Variants Scraper free?
NCBI ClinVar Variants Scraper is not fully free, but Apify provides a free tier so you can test it before paying for usage.
How to use NCBI ClinVar Variants Scraper?
Open NCBI ClinVar Variants Scraper on Apify, configure the input for the data you want to scrape, run the actor, and export the results when the run completes.
Free tier available. No credit card needed.
We earn commission from qualifying purchases. This does not affect our ratings.
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