"GeneDx"[submitter] AND "SGCZ"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59735	GRCh38/hg38 8p23.3-12(chr8:96310-30614703)x3	ADAM28, ADAM7 +979 more	Copy number gain	See cases	GPathogenic
Select item 152909	GRCh38/hg38 8p23.3-12(chr8:226452-34491890)x3	LOC130000099, LOC130000100 +1040 more	Copy number gain	See cases	GPathogenic
Select item 59766	GRCh38/hg38 8p23.1-11.1(chr8:12750796-43532444)x3	ADAM18, ADAM2 +922 more	Copy number gain	See cases	GPathogenic
Select item 58403	GRCh38/hg38 8p22(chr8:13421415-14228782)x3	C8orf48, DLC1 +23 more	Copy number gain	See cases	GUncertain significance
Select item 152379	GRCh38/hg38 8p22(chr8:14047934-14103793)x3	SGCZ	Copy number gain	See cases	GBenign
Select item 145248	GRCh38/hg38 8p22(chr8:14714802-14757672)x1	SGCZ	Copy number loss	See cases	GBenign
Select item 59769	GRCh38/hg38 8p22-q11.21(chr8:14940110-47929925)x3	LOC130000309, LOC130000310 +900 more	Copy number gain	See cases	GPathogenic
Select item 151537	GRCh38/hg38 8p22(chr8:14940111-14976577)x3	SGCZ	Copy number gain	See cases	GBenign
Select item 253392	GRCh37/hg19 8p23.1-21.2(chr8:12580132-26774307)x3	ADAM28, ADAM7 +82 more	Copy number gain	See cases	GPathogenic

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