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

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685986	GRCh37/hg19 4q26-32.3(chr4:117518683-168174703)x3	SPOCK3, SPRY1 +153 more	Copy number gain	not provided	GPathogenic
Select item 2684399	GRCh37/hg19 4q32.3-35.2(chr4:167409608-190957473)x3	AADAT, ACSL1 +69 more	Copy number gain	not provided	GPathogenic
Select item 1808805	GRCh37/hg19 4q32.3(chr4:167428990-167860888)x3	SPOCK3	Copy number gain	not provided	GUncertain significance
Select item 1341239	GRCh37/hg19 4q32.3(chr4:168034701-168115705)x1	SPOCK3	Copy number loss	not provided	GUncertain significance
Select item 1340412	GRCh37/hg19 4q32.3(chr4:166474584-167663163)x1	SPOCK3, TLL1	Copy number loss	not provided	GUncertain significance
Select item 980707	GRCh37/hg19 4q32.3(chr4:167817512-168996168)x1	SPOCK3	Copy number loss	not provided	GUncertain significance
Select item 814626	GRCh37/hg19 4q32.3(chr4:167490481-167693089)x3	SPOCK3	Copy number gain	not provided	GUncertain significance
Select item 814624	GRCh37/hg19 4q32.3(chr4:166967503-167656201)x3	SPOCK3, TLL1	Copy number gain	not provided	GUncertain significance
Select item 814622	GRCh37/hg19 4q32.3-35.2(chr4:165010461-190957473)x1	SCRG1, SH3RF1 +79 more	Copy number loss	not provided	GPathogenic
Select item 562989	GRCh37/hg19 4q32.1-35.2(chr4:159492464-190957473)x3	AADAT, ACSL1 +92 more	Copy number gain	not provided	GPathogenic
Select item 562986	GRCh37/hg19 4q32.1-35.1(chr4:157552397-183831253)x3	AADAT, ADAM29 +60 more	Copy number gain	not provided	GPathogenic