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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685308	GRCh37/hg19 8p11.21(chr8:42274264-42307548)x1	SLC20A2	Copy number loss	not provided	GPathogenic
Select item 2684529	GRCh37/hg19 8p22-11.1(chr8:14240573-43824035)x3	ADAM18, ADAM2 +176 more	Copy number gain	not provided	GPathogenic
Select item 1807741	GRCh37/hg19 8p11.21(chr8:42303398-43002481)x1	CHRNA6, CHRNB3 +8 more	Copy number loss	not provided	GPathogenic
Select item 815123	GRCh37/hg19 8p11.21(chr8:42143121-42353003)x3	DKK4, IKBKB +3 more	Copy number gain	not provided	GUncertain significance
Select item 563508	GRCh37/hg19 8p11.21(chr8:42303397-43002481)x1	FNTA, SMIM19 +8 more	Copy number loss	not provided	GPathogenic
Select item 563423	GRCh37/hg19 8p11.21(chr8:42301152-42354257)x1	SLC20A2	Copy number loss	not provided	GLikely pathogenic

ClinVar