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

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685211	GRCh37/hg19 6q15-21(chr6:92468126-109410569)x1	AFG1L, ARMC2 +43 more	Copy number loss	not provided	GPathogenic
Select item 2684449	GRCh37/hg19 6q16.3(chr6:100914616-101189581)x3	ASCC3	Copy number gain	not provided	GUncertain significance
Select item 1807838	GRCh37/hg19 6q16.1-21(chr6:96596732-105554568)x1	ASCC3, BVES +21 more	Copy number loss	not provided	GPathogenic
Select item 1807814	GRCh37/hg19 6q16.1-21(chr6:96946110-106497526)x1	ASCC3, BVES +22 more	Copy number loss	not provided	GPathogenic
Select item 1340754	GRCh37/hg19 6q16.3(chr6:101300165-101356389)x1	ASCC3	Copy number loss	not provided	GUncertain significance
Select item 816615	GRCh37/hg19 6q16.3(chr6:101195502-101520675)x1	ASCC3	Copy number loss	not provided	GUncertain significance
Select item 816614	GRCh37/hg19 6q16.3(chr6:101118288-101216562)x1	ASCC3	Copy number loss	not provided	GUncertain significance
Select item 814854	GRCh37/hg19 6q16.3(chr6:100900208-101204425)x3	ASCC3, SIM1	Copy number gain	not provided	GUncertain significance
Select item 814853	GRCh37/hg19 6q16.3(chr6:100655749-101365268)x3	ASCC3, SIM1	Copy number gain	not provided	GUncertain significance
Select item 563212	GRCh37/hg19 6q16.3(chr6:101127431-103281283)x1	GRIK2, ASCC3	Copy number loss	not provided	GUncertain significance
Select item 563211	GRCh37/hg19 6q16.3(chr6:101091433-102152010)x3	ASCC3, GRIK2	Copy number gain	not provided	GUncertain significance
Select item 563204	GRCh37/hg19 6q16.1-22.1(chr6:95549951-116684929)x1	AFG1L, AK9 +80 more	Copy number loss	not provided	GPathogenic