ClinVar for Gene (Select 102659288) - ClinVar

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Links from Gene

Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 157041	Single allele	LINC02888, LOC126859952	Deletion	Gestational diabetes mellitus uncontrolled +1 more	Gnot provided
Select item 155519	GRCh38/hg38 7p22.3-15.2(chr7:43360-27196404)x3	LOC129998085, LOC129998086 +904 more	Copy number gain	See cases	GPathogenic
Select item 154993	GRCh38/hg38 7p22.3-15.2(chr7:1698124-27207295)x3	ABCB5, ACTB +769 more	Copy number gain	See cases	GPathogenic
Select item 154641	GRCh38/hg38 7p21.3-15.2(chr7:10610069-25760560)x1	LOC129998072, LOC129998073 +331 more	Copy number loss	See cases	GPathogenic
Select item 151570	GRCh38/hg38 7p21.1(chr7:17238688-17474079)x3	AHR, LINC02888 +6 more	Copy number gain	See cases	GBenign
Select item 149095	GRCh38/hg38 7p21.1(chr7:17198359-17893255)x3	AHR, LINC02888 +13 more	Copy number gain	See cases	GUncertain significance
Select item 148859	GRCh38/hg38 7p21.2-15.3(chr7:15533812-24851432)x1	ABCB5, AGMO +248 more	Copy number loss	See cases	GPathogenic
Select item 148758	GRCh38/hg38 7p22.3-15.3(chr7:45130-25221165)x3	RAC1, RADIL +823 more	Copy number gain	See cases	GPathogenic
Select item 148160	GRCh38/hg38 7p21.2-21.1(chr7:16121516-20607899)x1	AGR2, AGR3 +84 more	Copy number loss	See cases	GPathogenic
Select item 147798	GRCh38/hg38 7p21.1(chr7:17214494-17893255)x3	AHR, LINC02888 +13 more	Copy number gain	See cases	GUncertain significance
Select item 147793	GRCh38/hg38 7p21.2-21.1(chr7:13966197-18321354)x1	AGMO, AGR2 +59 more	Copy number loss	See cases	GPathogenic
Select item 147466	GRCh38/hg38 7p22.1-15.2(chr7:5682209-27230311)x3	ABCB5, AGMO +560 more	Copy number gain	See cases	GPathogenic
Select item 147424	GRCh38/hg38 7p21.1(chr7:17214494-18000678)x3	AHR, LINC02888 +13 more	Copy number gain	See cases	GUncertain significance
Select item 147357	GRCh38/hg38 7p22.3-15.2(chr7:54185-26827634)x3	HYCC1, ICA1 +879 more	Copy number gain	See cases	GPathogenic
Select item 146209	GRCh38/hg38 7p21.1(chr7:16838053-17663993)x3	AGR3, AHR +16 more	Copy number gain	See cases	GUncertain significance
Select item 146075	GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	CUL1, CUX1 +4737 more	Copy number loss	See cases	GPathogenic
Select item 59679	GRCh38/hg38 7p21.2-15.2(chr7:16234212-26167278)x3	ABCB5, AGR2 +287 more	Copy number gain	See cases	GPathogenic
Select item 59678	GRCh38/hg38 7p22.3-14.2(chr7:54185-37089712)x3	LOC129998210, LOC129998211 +1148 more	Copy number gain	See cases	GPathogenic
Select item 59570	GRCh38/hg38 7p21.1(chr7:17183146-17612077)x3	AHR, LINC02888 +10 more	Copy number gain	See cases	GUncertain significance
Select item 59569	GRCh38/hg38 7p21.1(chr7:17034713-17544671)x3	AHR, LINC02888 +11 more	Copy number gain	See cases	GUncertain significance
Select item 59568	GRCh38/hg38 7p21.1(chr7:16838053-17672667)x3	AGR3, AHR +16 more	Copy number gain	See cases	GUncertain significance
Select item 58520	GRCh38/hg38 7p21.2-21.1(chr7:15133711-19642829)x1	AGMO, AGR2 +67 more	Copy number loss	See cases	GPathogenic
Select item 58518	GRCh38/hg38 7p21.3-21.1(chr7:9975653-19356878)x1	AGMO, AGR2 +130 more	Copy number loss	See cases	GPathogenic
Select item 57453	GRCh38/hg38 7p22.3-14.1(chr7:54185-41875885)x3	ABCB5, ACTB +1298 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 24