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

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685557	GRCh37/hg19 16p13.13-13.12(chr16:11444572-12722447)x1	BCAR4, GSPT1 +8 more	Copy number loss	not provided	GUncertain significance
Select item 2684788	GRCh37/hg19 16p13.13-13.12(chr16:12229416-12915390)x3	CPPED1, SNX29	Copy number gain	not provided	GUncertain significance
Select item 1809399	GRCh37/hg19 16p13.13(chr16:12007435-12073710)x1	GSPT1, SNX29 +1 more	Copy number loss	not provided	GUncertain significance
Select item 1809030	GRCh37/hg19 16p13.2-13.13(chr16:10423631-12176517)x3	CIITA, ATF7IP2 +21 more	Copy number gain	not provided	GUncertain significance
Select item 1808469	GRCh37/hg19 16p13.13(chr16:12170523-12374728)x3	SNX29	Copy number gain	not provided	GUncertain significance
Select item 1807793	GRCh37/hg19 16p13.3-11.2(chr16:4380767-30445350)x3	ABAT, ABCC1 +226 more	Copy number gain	not provided	GPathogenic
Select item 1340789	GRCh37/hg19 16p13.13(chr16:12278972-12338544)x1	SNX29	Copy number loss	not provided	GLikely benign
Select item 1340054	GRCh37/hg19 16p13.13(chr16:12007434-12085776)x1	GSPT1, SNX29 +1 more	Copy number loss	not provided	GUncertain significance
Select item 980563	GRCh37/hg19 16p13.13(chr16:12039345-12256698)x3	SNX29, TNFRSF17	Copy number gain	not provided	GUncertain significance
Select item 980086	GRCh37/hg19 16p13.13(chr16:12117856-12374728)x3	SNX29	Copy number gain	not provided	GUncertain significance
Select item 980084	GRCh37/hg19 16p13.13(chr16:12204015-12420150)x1	SNX29	Copy number loss	not provided	GLikely benign
Select item 564276	GRCh37/hg19 16p13.13(chr16:12327596-12397665)x1	SNX29	Copy number loss	not provided	GLikely benign
Select item 564275	GRCh37/hg19 16p13.13(chr16:12120389-12452622)x1	SNX29	Copy number loss	not provided	GLikely benign
Select item 564274	GRCh37/hg19 16p13.13-13.12(chr16:12007434-14781381)x1	BFAR, CPPED1 +10 more	Copy number loss	not provided	GUncertain significance
Select item 564273	GRCh37/hg19 16p13.13(chr16:11954001-12161925)x3	GSPT1, TNFRSF17 +1 more	Copy number gain	not provided	GUncertain significance