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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685237	GRCh37/hg19 7p21.1-15.3(chr7:18603745-21437047)x1	ABCB5, FERD3L +7 more	Copy number loss	not provided	GPathogenic
Select item 2685236	GRCh37/hg19 7p21.1(chr7:18168602-18226800)x1	HDAC9	Copy number loss	not provided	GUncertain significance
Select item 1808624	GRCh37/hg19 7p21.1(chr7:18503934-19516395)x3	FERD3L, HDAC9 +1 more	Copy number gain	not provided	GUncertain significance
Select item 1807625	GRCh37/hg19 7p21.1(chr7:18954983-19024233)x1	HDAC9	Copy number loss	not provided	GUncertain significance
Select item 980247	GRCh37/hg19 7p21.2-21.1(chr7:16279316-18429845)x1	SOSTDC1, AGR2 +10 more	Copy number loss	not provided	GUncertain significance
Select item 979766	GRCh37/hg19 7p21.1(chr7:17865965-18361645)x3	PRPS1L1, SNX13 +1 more	Copy number gain	not provided	GLikely benign
Select item 814934	GRCh37/hg19 7p21.2-21.1(chr7:13886653-20267202)x1	MEOX2, PRPS1L1 +19 more	Copy number loss	not provided	GPathogenic
Select item 563419	GRCh37/hg19 7p21.2-15.3(chr7:14544155-21719929)x3	AGR3, TSPAN13 +23 more	Copy number gain	not provided	GPathogenic
Select item 563393	GRCh37/hg19 7p21.1(chr7:17008842-18304130)x3	HDAC9, SNX13 +2 more	Copy number gain	not provided	GUncertain significance
Select item 563335	GRCh37/hg19 7p21.1(chr7:18149462-18471405)x1	HDAC9	Copy number loss	not provided	GLikely benign