"GeneDx"[submitter] AND "ADCY2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58069	GRCh38/hg38 5p15.33-15.31(chr5:3075612-7650835)x3	ADAMTS16, ADAMTS16-DT +91 more	Copy number gain	See cases	GPathogenic
Select item 144887	GRCh38/hg38 5p15.31(chr5:7422048-7449225)x3	ADCY2	Copy number gain	See cases	GBenign
Select item 1235804	NM_020546.3(ADCY2):c.2094+6T>C	ADCY2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281229	NM_020546.3(ADCY2):c.2094+16C>T	ADCY2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1302453	NM_020546.3(ADCY2):c.2661C>T (p.Cys887=)	ADCY2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 253596	GRCh37/hg19 5p15.33-15.2(chr5:22149-13362684)x1	ADAMTS16, ADCY2 +49 more	Copy number loss	See cases	GPathogenic
Select item 253537	GRCh37/hg19 5p15.33-13.2(chr5:22149-34041255)x3	AHRR, ADAMTS12 +82 more	Copy number gain	See cases	GPathogenic
Select item 253478	GRCh37/hg19 5p15.33-15.1(chr5:79146-15509107)x1	ADAMTS16, ADCY2 +56 more	Copy number loss	See cases	GPathogenic

ClinVar