"GeneDx"[submitter] AND "LOC101927506"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151543	GRCh38/hg38 8p23.3(chr8:66046-123860)x3	LOC101927506	Copy number gain	See cases	GBenign
Select item 145217	GRCh38/hg38 8p23.3(chr8:66046-106814)x3	LOC101927506	Copy number gain	See cases	GBenign
Select item 152332	GRCh38/hg38 8p23.3(chr8:70977-144623)x3	LOC101927506	Copy number gain	See cases	GBenign
Select item 145724	GRCh38/hg38 8p23.3(chr8:90247-106814)x3	LOC101927506	Copy number gain	See cases	GBenign
Select item 144954	GRCh38/hg38 8p23.3(chr8:90247-178199)x3	LOC101927506, OR4F21	Copy number gain	See cases	GBenign
Select item 144951	GRCh38/hg38 8p23.3(chr8:90247-195465)x3	LOC101927506, OR4F21	Copy number gain	See cases	GBenign
Select item 59735	GRCh38/hg38 8p23.3-12(chr8:96310-30614703)x3	ADAM28, ADAM7 +979 more	Copy number gain	See cases	GPathogenic

ClinVar