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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685318	GRCh37/hg19 8q22.2-22.3(chr8:100446969-102315070)x1	ANKRD46, COX6C +10 more	Copy number loss	not provided	GUncertain significance
Select item 2684546	GRCh37/hg19 8q21.12-22.3(chr8:79046933-102008860)x3	ANKRD46, ATP6V0D2 +96 more	Copy number gain	not provided	GPathogenic
Select item 1809446	GRCh37/hg19 8q22.2(chr8:100791384-101278033)x3	COX6C, FBXO43 +5 more	Copy number gain	not provided	GUncertain significance
Select item 1808681	GRCh37/hg19 8q21.12-24.11(chr8:79409349-119040631)x3	AARD, ABRA +141 more	Copy number gain	not provided	GPathogenic
Select item 979846	GRCh37/hg19 8q22.2(chr8:101017828-101094066)x1	RGS22	Copy number loss	not provided	GUncertain significance
Select item 815149	GRCh37/hg19 8q22.2(chr8:100791383-101278033)x3	POLR2K, RNF19A +5 more	Copy number gain	not provided	GUncertain significance
Select item 563556	GRCh37/hg19 8q21.2-23.3(chr8:86841154-116518125)x3	DCAF13, CNGB3 +105 more	Copy number gain	not provided	GPathogenic
Select item 563534	GRCh37/hg19 8q22.2-22.3(chr8:100551211-103676738)x1	COX6C, UBR5 +17 more	Copy number loss	not provided	GPathogenic

ClinVar