"Urologic Oncology Branch, National Institutes of Health"[submitter] A - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 997741	NC_000003.12:g.10135142_10142466del	LOC107303339, LOC107303340 +1 more	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997740	NC_000003.12:g.10135142_10143568del	LOC107303340, LOC107303339 +1 more	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997742	NC_000003.12:g.10137026_10145481del	LOC107303340, LOC107303339 +1 more	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997743	NC_000003.12:g.10137102_10143357del	LOC107303339, LOC107303340 +1 more	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997746	NC_000003.12:g.10139220_10148953del	LOC107303340, VHL	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997747	NC_000003.12:g.10139708_10142406del	LOC107303340, VHL	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997748	NC_000003.12:g.10139761_10142459del	LOC107303340, VHL	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997750	NC_000003.12:g.10140648_10148414del	LOC107303340, VHL	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997754	NC_000003.12:g.10140738_10142535del	LOC107303340, VHL	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997755	NC_000003.12:g.10141523_10142610del	LOC107303340, VHL	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997757	NM_000551.4(VHL):c.340+221_464-1411del	LOC107303340, VHL	Deletion (splice acceptor variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997758	NM_000551.4(VHL):c.340+283_463+499del	LOC107303340, VHL	Deletion (splice acceptor variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997759	NM_000551.4(VHL):c.340+307_464-1191del	LOC107303340, VHL	Deletion (splice acceptor variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997721	NM_000551.4(VHL):c.340+365_464-909del	LOC107303340, VHL	Deletion (splice acceptor variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997722	NM_000551.4(VHL):c.340+428_464-1203del	LOC107303340, VHL	Deletion (intron variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997723	NM_000551.4(VHL):c.340+444_464-1187del	LOC107303340, VHL	Deletion (splice acceptor variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997724	NM_000551.4(VHL):c.340+994_*2333del	LOC107303340, VHL	Deletion (splice acceptor variant +1 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997725	NM_000551.4(VHL):c.340+1019_463+450del	LOC107303340, VHL	Deletion (intron variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997726	NM_000551.4(VHL):c.340+1543_464-1191del	LOC107303340, VHL	Deletion (intron variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997727	NM_000551.4(VHL):c.340+1580_464-1477del	LOC107303340, VHL	Deletion (intron variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997728	NM_000551.4(VHL):c.341-1857_464-1328del	LOC107303340, VHL	Deletion (intron variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997729	NM_000551.4(VHL):c.341-1583_464-1477del	LOC107303340, VHL	Deletion (intron variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997730	NM_000551.4(VHL):c.341-1406_*3377del	LOC107303340, VHL	Deletion (splice acceptor variant +1 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997731	NM_000551.4(VHL):c.341-1382_*3401del	LOC107303340, VHL	Deletion (splice acceptor variant +1 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997732	NM_000551.4(VHL):c.341-951_464-1018del	LOC107303340, VHL	Deletion (intron variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997733	NM_000551.4(VHL):c.341-929_*3191del	LOC107303340, VHL	Deletion (splice acceptor variant +1 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997734	NM_000551.4(VHL):c.341-279_464-614del	LOC107303340, VHL	Deletion (intron variant +2 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997752	NM_000551.4(VHL):c.341-49_*2815del	LOC107303340, VHL	Deletion (splice acceptor variant +1 more)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997753	NM_000551.4(VHL):c.463+439_*991del	LOC107303340, VHL	Deletion (splice acceptor variant)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997762	NM_000551.4(VHL):c.463+1008_*2803del	LOC107303340, VHL	Deletion (splice acceptor variant)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997764	NC_000003.12:g.10148440_10158273del	LOC107303340, VHL	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997765	NC_000003.12:g.10148566_10158401del	LOC107303340, VHL	Deletion	Von Hippel-Lindau syndrome	GPathogenic
Select item 997767	NM_000551.4(VHL):c.464-1226_*2771del	LOC107303340, VHL	Deletion (splice acceptor variant)	Von Hippel-Lindau syndrome	GPathogenic
Select item 997766	NC_000003.12:g.10148615_10158450del	LOC107303340, VHL	Deletion	Von Hippel-Lindau syndrome	GPathogenic

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Items: 34