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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685604	GRCh37/hg19 17q23.1-23.2(chr17:58111095-60355640)x1	APPBP2, BCAS3 +12 more	Copy number loss	not provided	GPathogenic
Select item 1340823	GRCh37/hg19 17q23.1-23.2(chr17:57605300-59389547)x1	APPBP2, BCAS3 +13 more	Copy number loss	not provided	GPathogenic
Select item 1340122	GRCh37/hg19 17q23.2(chr17:58932118-59022605)x1	BCAS3	Copy number loss	not provided	GUncertain significance
Select item 980724	GRCh37/hg19 17q23.2(chr17:58713087-59030337)x1	BCAS3, PPM1D	Copy number loss	not provided	GUncertain significance
Select item 815945	GRCh37/hg19 17q23.2(chr17:58857083-59054823)x1	BCAS3	Copy number loss	not provided	GUncertain significance
Select item 564459	GRCh37/hg19 17q23.2(chr17:59058222-59352951)x4	BCAS3	Copy number gain	not provided	GUncertain significance
Select item 564458	GRCh37/hg19 17q23.2(chr17:58521331-58916828)x3	BCAS3, APPBP2 +1 more	Copy number gain	not provided	GUncertain significance
Select item 564457	GRCh37/hg19 17q23.2(chr17:58388728-60486746)x1	BCAS3, LINC02875 +11 more	Copy number loss	not provided	GLikely pathogenic

ClinVar