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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2684620	GRCh37/hg19 2p12(chr2:79773859-80062710)x1	CTNNA2	Copy number loss	not provided	GUncertain significance
Select item 1807933	GRCh37/hg19 2p12(chr2:80338539-80777211)x1	CTNNA2, LRRTM1	Copy number loss	not provided	GUncertain significance
Select item 1807862	GRCh37/hg19 2p12(chr2:80732592-80805828)x1	CTNNA2	Copy number loss	not provided	GUncertain significance
Select item 1341180	GRCh37/hg19 2p12(chr2:79888287-82209482)x3	CTNNA2, LRRTM1	Copy number gain	not provided	GUncertain significance
Select item 980973	GRCh37/hg19 2p12(chr2:76035305-81220405)x1	CTNNA2, LRRTM1 +5 more	Copy number loss	not provided	GUncertain significance
Select item 814277	GRCh37/hg19 2p12(chr2:80105358-80209568)x1	CTNNA2	Copy number loss	not provided	GUncertain significance
Select item 814276	GRCh37/hg19 2p12(chr2:79491432-79805562)x3	CTNNA2	Copy number gain	not provided	GUncertain significance
Select item 562678	GRCh37/hg19 2p13.1-11.2(chr2:74527522-89125488)x1	ATOH8, AUP1 +78 more	Copy number loss	not provided	GPathogenic

ClinVar