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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1807798	GRCh37/hg19 6q26-27(chr6:163181847-170919482)x1	AFDN, C6orf118 +32 more	Copy number loss	not provided	GPathogenic
Select item 979588	GRCh37/hg19 6q26(chr6:163285982-163505631)x3	PACRG	Copy number gain	not provided	GUncertain significance
Select item 979582	GRCh37/hg19 6q26(chr6:162680773-163427383)x1	PRKN, PACRG	Copy number loss	not provided	GLikely benign
Select item 814903	GRCh37/hg19 6q26(chr6:162765163-163266877)x3	PACRG, PRKN	Copy number gain	not provided	GUncertain significance
Select item 814901	GRCh37/hg19 6q26-27(chr6:162661108-170919482)x1	CEP43, DACT2 +33 more	Copy number loss	not provided	GPathogenic
Select item 814897	GRCh37/hg19 6q26-27(chr6:162452035-170919482)x1	GPR31, KIF25 +33 more	Copy number loss	not provided	GPathogenic
Select item 563252	GRCh37/hg19 6q26(chr6:162693562-163399349)x3	PRKN, PACRG	Copy number gain	not provided	GUncertain significance
Select item 563245	GRCh37/hg19 6q25.3-27(chr6:159844762-170919482)x3	ACAT2, AFDN +49 more	Copy number gain	not provided	GPathogenic

ClinVar