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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 979973	GRCh37/hg19 2p22.3-22.2(chr2:36432453-38182274)x3	CRIM1, SULT6B1 +12 more	Copy number gain	not provided	GUncertain significance
Select item 979967	GRCh37/hg19 2p22.2(chr2:36850479-37013926)x1	VIT	Copy number loss	not provided	GUncertain significance
Select item 814234	GRCh37/hg19 2p22.2(chr2:37003199-37121056)x1	VIT, STRN	Copy number loss	not provided	GUncertain significance
Select item 562680	GRCh37/hg19 2p22.3-16.1(chr2:34792916-56676541)x3	ABCG5, ABCG8 +100 more	Copy number gain	not provided	GPathogenic
Select item 562540	GRCh37/hg19 2p22.2(chr2:36804289-37006684)x3	VIT, FEZ2	Copy number gain	not provided	GUncertain significance
Select item 562498	GRCh37/hg19 2p22.2(chr2:36957586-37029623)x1	VIT	Copy number loss	not provided	GUncertain significance

ClinVar