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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1341211	GRCh37/hg19 4q21.21-22.1(chr4:80467886-93362064)x1	ABCG2, ABRAXAS1 +58 more	Copy number loss	not provided	GPathogenic
Select item 1340655	GRCh37/hg19 4q22.1(chr4:89782569-89849657)x1	FAM13A	Copy number loss	not provided	GLikely benign
Select item 1340288	GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	AASDH, ABCG2 +359 more	Copy number gain	not provided	GPathogenic
Select item 814582	GRCh37/hg19 4q22.1(chr4:89790888-90586088)x1	GPRIN3, TIGD2 +1 more	Copy number loss	not provided	GUncertain significance
Select item 562944	GRCh37/hg19 4q22.1(chr4:89811514-89938991)x1	FAM13A	Copy number loss	not provided	GUncertain significance
Select item 562937	GRCh37/hg19 4q21.21-22.3(chr4:81314915-96636651)x1	ABCG2, ABRAXAS1 +60 more	Copy number loss	not provided	GPathogenic

ClinVar