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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685114	GRCh37/hg19 4q13.2-13.3(chr4:69146217-75500577)x1	ADAMTS3, AFM +58 more	Copy number loss	not provided	GPathogenic
Select item 1340436	GRCh37/hg19 4q13.3(chr4:72998352-73320894)x3	ADAMTS3, NPFFR2	Copy number gain	not provided	GUncertain significance
Select item 1340288	GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	AASDH, ABCG2 +359 more	Copy number gain	not provided	GPathogenic
Select item 980093	GRCh37/hg19 4q13.3(chr4:73222936-73389169)x1	ADAMTS3	Copy number loss	not provided	GLikely benign
Select item 814568	GRCh37/hg19 4q13.3(chr4:73184648-73813059)x3	ADAMTS3	Copy number gain	not provided	GUncertain significance
Select item 814567	GRCh37/hg19 4q13.3(chr4:72834889-73561412)x3	NPFFR2, ADAMTS3	Copy number gain	not provided	GUncertain significance
Select item 814566	GRCh37/hg19 4q13.3-21.23(chr4:72680879-86426232)x1	CXCL3, LIN54 +82 more	Copy number loss	not provided	GPathogenic
Select item 814563	GRCh37/hg19 4q13.2-21.21(chr4:68950363-79738598)x1	ADAMTS3, AFM +92 more	Copy number loss	not provided	GPathogenic
Select item 562920	GRCh37/hg19 4q13.1-13.3(chr4:64705501-73469716)x3	ADAMTS3, AMBN +49 more	Copy number gain	not provided	GPathogenic

ClinVar