ClinVar Miner

Submissions for variant GRCh37/hg19 10q24.31-24.32(chr10:102822575-103558868)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV000767666 SCV000898288 pathogenic Split hand-foot malformation 3 2018-11-01 criteria provided, single submitter clinical testing This CNV was detected in a symptomatic patient referred for CMA testing, but consent was not obtained to report individual clinical features

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.