"GeneDx"[submitter] AND "IRF7"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151263	GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3	DENND5A, DNHD1 +723 more	Copy number gain	See cases	GPathogenic
Select item 59748	GRCh38/hg38 11p15.5-15.4(chr11:218365-3377077)x3	ANO9, AP2A2 +266 more	Copy number gain	See cases	GPathogenic
Select item 1170389	NM_001572.5(IRF7):c.327G>A (p.Arg109=)	IRF7	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign
Select item 1170390	NM_001572.5(IRF7):c.184-3C>A	IRF7	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 1170391	NM_001572.5(IRF7):c.184-4T>A	IRF7	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 253876	GRCh37/hg19 11p15.5(chr11:532230-699463)x3	CDHR5, DEAF1 +12 more	Copy number gain	See cases	GUncertain significance

ClinVar