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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685260	GRCh37/hg19 7q22.3-31.1(chr7:104536649-109624996)x1	ATXN7L1, BCAP29 +26 more	Copy number loss	not provided	GPathogenic
Select item 2684503	GRCh37/hg19 7q31.1(chr7:107981349-110641907)x3	DNAJB9, IMMP2L +4 more	Copy number gain	not provided	GUncertain significance
Select item 979641	GRCh37/hg19 7q31.1(chr7:108025055-108085810)x1	NRCAM	Copy number loss	not provided	GUncertain significance
Select item 815016	GRCh37/hg19 7q31.1(chr7:108094786-108494963)x3	PNPLA8, DNAJB9 +2 more	Copy number gain	not provided	GLikely benign
Select item 815015	GRCh37/hg19 7q31.1(chr7:107441501-108433812)x1	PNPLA8, DLD +6 more	Copy number loss	not provided	GUncertain significance
Select item 815014	GRCh37/hg19 7q22.3-31.32(chr7:106617406-123217914)x1	TMEM168, LAMB4 +59 more	Copy number loss	not provided	GPathogenic
Select item 563422	GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3	AASS, ABCB8 +436 more	Copy number gain	not provided	GPathogenic

ClinVar