"GeneDx"[submitter] AND "CPNE7"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58270	GRCh38/hg38 16q24.3(chr16:89570545-89814613)x1	CDK10, CHMP1A +35 more	Copy number loss	See cases	GUncertain significance
Select item 152598	GRCh38/hg38 16q24.3(chr16:89582242-89623414)x3	CPNE7, DPEP1	Copy number gain	See cases	GBenign/Likely benign
Select item 152584	GRCh38/hg38 16q24.3(chr16:89582242-89635475)x3	CPNE7, DPEP1 +1 more	Copy number gain	See cases	GBenign/Likely benign
Select item 151638	GRCh38/hg38 16q24.3(chr16:89582242-89593912)x3	CPNE7	Copy number gain	See cases	GBenign
Select item 151644	GRCh38/hg38 16q24.3(chr16:89586679-89648483)x3	CHMP1A, CPNE7 +2 more	Copy number gain	See cases	GLikely benign
Select item 151822	GRCh38/hg38 16q24.3(chr16:89593912-89623414)x3	CPNE7, DPEP1	Copy number gain	See cases	GBenign/Likely benign
Select item 253986	GRCh37/hg19 16q24.2-24.3(chr16:88601532-89713753)x3	ACSF3, ANKRD11 +24 more	Copy number gain	See cases	GUncertain significance
Select item 253554	GRCh37/hg19 16q23.1-24.3(chr16:74872514-90274440)x3	ACSF3, ADAD2 +127 more	Copy number gain	See cases	GPathogenic

ClinVar