"Quest Diagnostics Nichols Institute San Juan Capistrano"[submitter] A - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684576	GRCh37/hg19 9p22.1(chr9:19189213-19437829)x3	ACER2, DENND4C +1 more	Copy number gain	not provided	GUncertain significance
Select item 2684569	GRCh37/hg19 9p24.3-13.1(chr9:1475882-38771831)x3	CREB3, STOML2 +188 more	Copy number gain	not provided	GPathogenic
Select item 1808046	GRCh37/hg19 9p22.3-21.3(chr9:15328600-20821644)x3	ACER2, ADAMTSL1 +15 more	Copy number gain	not provided	GUncertain significance
Select item 1340732	GRCh37/hg19 9p22.1(chr9:19328752-19535747)x3	ACER2, DENND4C +2 more	Copy number gain	not provided	GLikely benign
Select item 1340064	GRCh37/hg19 9p22.1(chr9:18987330-19413864)x3	ACER2, DENND4C +5 more	Copy number gain	not provided	GUncertain significance
Select item 980890	GRCh37/hg19 9p22.1(chr9:19108473-19329836)x1	DENND4C, PLIN2	Copy number loss	not provided	GUncertain significance
Select item 980354	GRCh37/hg19 9p22.1(chr9:19313795-19367790)x1	DENND4C	Copy number loss	not provided	GUncertain significance
Select item 980353	GRCh37/hg19 9p22.1(chr9:19289042-19526144)x3	DENND4C, RPS6 +2 more	Copy number gain	not provided	GLikely benign
Select item 815243	GRCh37/hg19 9p22.1(chr9:19283503-19569670)x3	SLC24A2, RPS6 +2 more	Copy number gain	not provided	GLikely benign
Select item 815242	GRCh37/hg19 9p22.1(chr9:19080351-19544088)x3	PLIN2, SLC24A2 +4 more	Copy number gain	not provided	GUncertain significance
Select item 815190	GRCh37/hg19 9p24.3-q21.11(chr9:203861-70984588)x3	ACER2, ACO1 +213 more	Copy number gain	not provided	GPathogenic
Select item 563687	GRCh37/hg19 9p24.3-q21.12(chr9:203861-72717793)x3	ACER2, ACO1 +225 more	Copy number gain	not provided	GPathogenic
Select item 563686	GRCh37/hg19 9p24.3-q21.11(chr9:203861-70985795)x4	ACER2, ACO1 +213 more	Copy number gain	not provided	GPathogenic
Select item 563685	GRCh37/hg19 9p24.3-q13(chr9:203861-68262804)x3,4	CNTNAP3, CNTNAP3B +204 more	Copy number gain	not provided	GPathogenic
Select item 563684	GRCh37/hg19 9p24.3-q13(chr9:203861-67983174)x4	ATOSB, B4GALT1 +204 more	Copy number gain	not provided	GPathogenic
Select item 563683	GRCh37/hg19 9p24.3-13.1(chr9:203861-38787480)x3	DMAC1, DMRT1 +194 more	Copy number gain	not provided	GPathogenic
Select item 563682	GRCh37/hg19 9p24.3-21.2(chr9:203861-26397133)x3	DMAC1, TYRP1 +89 more	Copy number gain	not provided	GPathogenic
Select item 563681	GRCh37/hg19 9p24.3-21.3(chr9:203861-20653468)x3	ZDHHC21, ACER2 +61 more	Copy number gain	not provided	GPathogenic
Select item 563661	GRCh37/hg19 9p22.1-21.3(chr9:18944282-19964747)x3	RRAGA, SAXO1 +6 more	Copy number gain	not provided	GUncertain significance
Select item 563650	GRCh37/hg19 9p22.1(chr9:18935985-19603778)x3	RRAGA, RPS6 +6 more	Copy number gain	not provided	GUncertain significance
Select item 563577	GRCh37/hg19 9p22.1(chr9:19236488-19322101)x1	DENND4C	Copy number loss	not provided	GUncertain significance

ClinVar

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Items: 21