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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809264	GRCh37/hg19 1q25.3-32.3(chr1:181453460-213107248)x3	ASPM, IPO9 +211 more	Copy number gain	not provided	GPathogenic
Select item 1808632	GRCh37/hg19 1q25.2-31.2(chr1:179727182-192260142)x1	ACBD6, APOBEC4 +48 more	Copy number loss	not provided	GPathogenic
Select item 1341276	GRCh37/hg19 1q25.2-31.1(chr1:178522021-190322133)x1	ABL2, ACBD6 +56 more	Copy number loss	not provided	GPathogenic
Select item 979312	GRCh37/hg19 1q25.3(chr1:183917739-184192431)x3	TSEN15, COLGALT2	Copy number gain	not provided	GUncertain significance
Select item 814148	GRCh37/hg19 1q25.3(chr1:183908612-183981164)x1	COLGALT2	Copy number loss	not provided	GUncertain significance
Select item 814145	GRCh37/hg19 1q25.2-32.1(chr1:177551193-199599056)x1	ABL2, ACBD6 +88 more	Copy number loss	not provided	GPathogenic
Select item 565205	GRCh37/hg19 1q25.3(chr1:183827844-184317756)x3	COLGALT2, RGL1 +1 more	Copy number gain	not provided	GUncertain significance

ClinVar