The Mastermind Cited Variants Reference (CVR) contains annotations with the number of articles for each variant cited in the medical literature. This public dataset is most commonly used as an evidence filter for clinical actionability in genomic analysis pipelines (based on presence or lack of evidence in the literature) and a quick way to get insight into the literature for variant curation through links into the Mastermind Genomic Search Engine.
You can access the following dataset in BigQuery for data exploration and querying. The dataset contains separate tables with annotations using build GRCh37 and GRCh38. Genomenon hosts a public repository with convenience scripts and information about how to directly annotate your variant data with the annotations from the public dataset.
About the dataset
Use: This dataset is publicly available for anyone to use under the terms provided by the dataset source (https://www.genomenon.com/cvr/) and is provided "AS IS" without any warranty, express or implied, from Google. Google disclaims all liability for any damages, direct or indirect, resulting from the use of the dataset.