ClinVar Miner

List of variants reported by Urologic Oncology Branch, National Institutes of Health

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NC_000003.11:g.10160443_10184298del
NC_000003.11:g.10167511_10193484del
NC_000003.11:g.10169230_10194915del
NC_000003.11:g.10170715_10188894del
NC_000003.11:g.10175778_10190168del
NC_000003.11:g.10175844_10187969del
NC_000003.11:g.10179846_10190051del
NC_000003.11:g.10180085_10190286del
NC_000003.11:g.10182212_10212738del
NC_000003.11:g.10184086_10218542del
NC_000003.11:g.10188005_10207561del
NC_000003.11:g.10188894_10200033del
NC_000003.11:g.10189293_10201409del
NC_000003.11:g.10189323_10202010del
NC_000003.11:g.10190033_10209132del
NC_000003.12:g.10135142_10142466del
NC_000003.12:g.10135142_10143568del
NC_000003.12:g.10137026_10145481del
NC_000003.12:g.10137102_10143357del
NC_000003.12:g.10139220_10148953del
NC_000003.12:g.10139708_10142406del
NC_000003.12:g.10139761_10142459del
NC_000003.12:g.10140148_10140759del rs1696067154
NC_000003.12:g.10140648_10148414del
NC_000003.12:g.10140738_10142535del
NC_000003.12:g.10141523_10142610del
NC_000003.12:g.10148440_10158273del
NC_000003.12:g.10148566_10158401del
NC_000003.12:g.10148615_10158450del
NM_000551.4(VHL):c.340+1019_463+450del
NM_000551.4(VHL):c.340+1543_464-1191del
NM_000551.4(VHL):c.340+1580_464-1477del
NM_000551.4(VHL):c.340+221_464-1411del
NM_000551.4(VHL):c.340+283_463+499del
NM_000551.4(VHL):c.340+307_464-1191del
NM_000551.4(VHL):c.340+365_464-909del
NM_000551.4(VHL):c.340+428_464-1203del
NM_000551.4(VHL):c.340+444_464-1187del
NM_000551.4(VHL):c.340+994_*2333del
NM_000551.4(VHL):c.341-1382_*3401del
NM_000551.4(VHL):c.341-1406_*3377del
NM_000551.4(VHL):c.341-1583_464-1477del
NM_000551.4(VHL):c.341-1857_464-1328del
NM_000551.4(VHL):c.341-279_464-614del
NM_000551.4(VHL):c.341-49_*2815del
NM_000551.4(VHL):c.341-929_*3191del
NM_000551.4(VHL):c.341-951_464-1018del
NM_000551.4(VHL):c.463+1008_*2803del
NM_000551.4(VHL):c.463+439_*991del
NM_000551.4(VHL):c.464-1226_*2771del

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.