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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1807899	GRCh37/hg19 7q31.32(chr7:121861729-121972691)x1	CADPS2, FEZF1	Copy number loss	not provided	GUncertain significance
Select item 979794	GRCh37/hg19 7q31.32(chr7:122009559-122111776)x1	CADPS2	Copy number loss	not provided	GUncertain significance
Select item 815028	GRCh37/hg19 7q31.32(chr7:122244359-122274997)x1	CADPS2	Copy number loss	not provided	GLikely pathogenic
Select item 815017	GRCh37/hg19 7q31.1-36.3(chr7:109251060-159119707)x3	CHRM2, KRBA1 +295 more	Copy number gain	not provided	GPathogenic
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