ClinVar Miner

Submissions for variant GRCh38/hg38 7q11.1-11.21(chr7:61006478-62410831)x3

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 7
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISCA site 15 RCV000051529 SCV000078877 uncertain significance See cases 2011-08-12 criteria provided, single submitter clinical testing
GeneDx RCV000051850 SCV000079198 pathogenic See cases 2011-08-12 criteria provided, single submitter clinical testing
GeneDx RCV000134697 SCV000174269 benign See cases 2010-11-30 no assertion criteria provided clinical testing
ISCA site 1 RCV000134991 SCV000174656 pathogenic See cases 2011-01-05 no assertion criteria provided clinical testing
ISCA site 4 RCV000136084 SCV000176126 benign/likely benign See cases 2012-09-21 no assertion criteria provided clinical testing Likely benign (1), Benign (1)
ISCA site 1 RCV000138200 SCV000178470 pathogenic See cases 2012-03-09 no assertion criteria provided clinical testing
GeneDx RCV000140087 SCV000180756 benign See cases 2011-04-30 no assertion criteria provided clinical testing

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.