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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685804	GRCh37/hg19 1p32.3(chr1:51284375-51569360)x3	C1orf185, CDKN2C +1 more	Copy number gain	not provided	GUncertain significance
Select item 2685432	GRCh37/hg19 1p32.3(chr1:51007512-51109162)x1	FAF1	Copy number loss	not provided	GUncertain significance
Select item 980377	GRCh37/hg19 1p32.3(chr1:51110292-51278635)x1	FAF1	Copy number loss	not provided	GUncertain significance
Select item 814081	GRCh37/hg19 1p32.3(chr1:51148897-51573845)x3	C1orf185, CDKN2C +1 more	Copy number gain	not provided	GUncertain significance
Select item 814080	GRCh37/hg19 1p32.3(chr1:51049896-51261965)x3	FAF1	Copy number gain	not provided	GUncertain significance
Select item 814074	GRCh37/hg19 1p33-32.3(chr1:47272184-52505405)x1	TXNDC12, AGBL4 +28 more	Copy number loss	not provided	GPathogenic
Select item 565095	GRCh37/hg19 1p32.3(chr1:51135986-51475942)x3	CDKN2C, FAF1	Copy number gain	not provided	GUncertain significance
Select item 565094	GRCh37/hg19 1p32.3(chr1:50978592-51238899)x1	FAF1	Copy number loss	not provided	GUncertain significance

ClinVar