ClinVar Miner

List of variants studied for syndrome caused by partial chromosomal deletion by Department of Medical Genetics, Oslo University Hospital

Included ClinVar conditions (110):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
GRCh37/hg19 17p13.3(chr17:84287-2468384)x1
GRCh37/hg19 1p32.3-31.3(chr1:53675707-66644963)x1
GRCh37/hg19 2q24.2-31.3(chr2:163078055-182119617)x1
GRCh37/hg19 2q37.1-37.3(chr2:233110452-243028452)x1
GRCh37/hg19 9p23-22.2(chr9:13638428-17121764)x1
GRCh37/hg19 9p24.3-22.2(chr9:204193-18073357)x1

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.