"GeneDx"[submitter] AND "PDE4B"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58079	GRCh38/hg38 1p32.3-31.1(chr1:52595352-76767765)x3	ACADM, ACOT11 +570 more	Copy number gain	See cases	GPathogenic
Select item 59970	GRCh38/hg38 1p32.2-31.1(chr1:57350574-71325924)x1	LOC111501769, LOC112590812 +339 more	Copy number loss	See cases	GPathogenic
Select item 59971	GRCh38/hg38 1p32.1-31.1(chr1:59632500-76730877)x1	ACADM, AK4 +331 more	Copy number loss	See cases	GPathogenic
Select item 58081	GRCh38/hg38 1p31.3(chr1:61922650-66445757)x3	AK4, ALG6 +129 more	Copy number gain	See cases	GPathogenic
Select item 59360	GRCh38/hg38 1p31.3(chr1:65969909-66128534)x1	PDE4B, PDE4B-AS1	Copy number loss	See cases	GUncertain significance
Select item 59361	GRCh38/hg38 1p31.3(chr1:66026161-66280387)x1	PDE4B, PDE4B-AS1	Copy number loss	See cases	GUncertain significance

ClinVar