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

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685214	GRCh37/hg19 6q22.31(chr6:123554219-125882578)x1	HDDC2, NKAIN2 +4 more	Copy number loss	not provided	GUncertain significance
Select item 2685213	GRCh37/hg19 6q22.31-23.3(chr6:120218852-137160850)x1	AHI1, AKAP7 +69 more	Copy number loss	not provided	GPathogenic
Select item 2685040	GRCh37/hg19 6q22.31(chr6:124918580-125201001)x4	NKAIN2	Copy number gain	not provided	GUncertain significance
Select item 1808541	GRCh37/hg19 6q22.31(chr6:121646369-124675332)x3	CLVS2, FABP7 +8 more	Copy number gain	not provided	GUncertain significance
Select item 1808088	GRCh37/hg19 6q22.31-22.33(chr6:120059951-130033233)x1	ARHGAP18, C6orf58 +27 more	Copy number loss	not provided	GUncertain significance
Select item 1808069	GRCh37/hg19 6q22.31(chr6:123858348-125320485)x1	NKAIN2, RNF217 +2 more	Copy number loss	not provided	GUncertain significance
Select item 1340790	GRCh37/hg19 6q22.31-22.33(chr6:125037475-129494795)x1	C6orf58, CENPW +17 more	Copy number loss	not provided	GPathogenic
Select item 980782	GRCh37/hg19 6q22.31(chr6:124632709-124755323)x1	NKAIN2	Copy number loss	not provided	GUncertain significance
Select item 563232	GRCh37/hg19 6q22.31(chr6:124691423-124984989)x3	NKAIN2	Copy number gain	not provided	GUncertain significance
Select item 563231	GRCh37/hg19 6q22.31(chr6:124496938-125189118)x3	NKAIN2	Copy number gain	not provided	GUncertain significance
Select item 563229	GRCh37/hg19 6q22.31(chr6:123509362-124332260)x3	NKAIN2, TRDN	Copy number gain	not provided	GUncertain significance