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

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 980348	GRCh37/hg19 9p21.2(chr9:26461273-27541041)x3	CAAP1, EQTN +5 more	Copy number gain	not provided	GUncertain significance
Select item 980347	GRCh37/hg19 9p21.2(chr9:26545337-27494803)x3	CAAP1, EQTN +5 more	Copy number gain	not provided	GUncertain significance
Select item 815253	GRCh37/hg19 9p21.2(chr9:27148497-27214342)x1	TEK	Copy number loss	not provided	GUncertain significance
Select item 815252	GRCh37/hg19 9p21.2(chr9:27009210-27226453)x3	IFT74, TEK	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 563625	GRCh37/hg19 9p21.2(chr9:27217431-27546449)x3	EQTN, MOB3B +1 more	Copy number gain	not provided	GUncertain significance