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

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809352	GRCh37/hg19 20p12.1(chr20:14054312-14622219)x3	FLRT3, MACROD2	Copy number gain	not provided	GUncertain significance
Select item 979567	GRCh37/hg19 20p12.1(chr20:14236417-14464775)x3	MACROD2, FLRT3	Copy number gain	not provided	GUncertain significance
Select item 979564	GRCh37/hg19 20p12.1(chr20:13432028-13987668)x3	MACROD2, TASP1 +3 more	Copy number gain	not provided	GUncertain significance
Select item 979563	GRCh37/hg19 20p12.1(chr20:14455496-14556385)x1	MACROD2	Copy number loss	not provided	GLikely benign
Select item 816119	GRCh37/hg19 20p12.1(chr20:15872280-16764799)x1	MACROD2, SNRPB2 +2 more	Copy number loss	not provided	GUncertain significance
Select item 816118	GRCh37/hg19 20p12.1(chr20:13390634-13990967)x3	ESF1, NDUFAF5 +3 more	Copy number gain	not provided	GUncertain significance
Select item 816114	GRCh37/hg19 20p12.3-11.22(chr20:8571696-22088650)x1	ANKEF1, BANF2 +49 more	Copy number loss	not provided	GPathogenic
Select item 816102	GRCh37/hg19 20p13-11.1(chr20:61568-26305479)x3	ABHD12, ACSS1 +177 more	Copy number gain	not provided	GPathogenic
Select item 564645	GRCh37/hg19 20p13-12.1(chr20:3092739-17091453)x1	FERMT1, SPTLC3 +62 more	Copy number loss	not provided	GPathogenic
Select item 564644	GRCh37/hg19 20p12.3-12.1(chr20:7604120-14739025)x3	BTBD3, TMX4 +18 more	Copy number gain	not provided	GPathogenic
Select item 564636	GRCh37/hg19 20p12.1(chr20:14797571-15693944)x1	MACROD2	Copy number loss	not provided	GLikely benign
Select item 564621	GRCh37/hg19 20p12.1(chr20:13845806-14137023)x3	SEL1L2, MACROD2	Copy number gain	not provided	GUncertain significance
Select item 564610	GRCh37/hg19 20p12.1(chr20:13984101-14057421)x1	MACROD2	Copy number loss	not provided	GLikely benign