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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685084	GRCh37/hg19 3p14.1(chr3:67611981-69023348)x1	SUCLG2, TAFA1 +1 more	Copy number loss	not provided	GUncertain significance
Select item 1809280	GRCh37/hg19 3p14.1(chr3:67449926-67622198)x1	SUCLG2	Copy number loss	not provided	GUncertain significance
Select item 1341307	GRCh37/hg19 3p14.2-13(chr3:59332508-70686155)x1	ADAMTS9, ARL6IP5 +24 more	Copy number loss	not provided	GPathogenic
Select item 1339990	GRCh37/hg19 3p14.1(chr3:67397253-68371598)x3	SUCLG2, TAFA1	Copy number gain	not provided	GUncertain significance
Select item 980500	GRCh37/hg19 3p14.1(chr3:67661612-67749080)x1	SUCLG2	Copy number loss	not provided	GLikely benign
Select item 562781	GRCh37/hg19 3p14.1-12.3(chr3:66133719-75076440)x1	ARL6IP5, CNTN3 +22 more	Copy number loss	not provided	GPathogenic

ClinVar