"GeneDx"[submitter] AND "MIR3667HG"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 57636	GRCh38/hg38 22q13.2-13.33(chr22:42433752-50738932)x1	A4GALT, ACR +521 more	Copy number loss	See cases	GPathogenic
Select item 57701	GRCh38/hg38 22q13.32-13.33(chr22:48138038-50739836)x1	ACR, ADM2 +211 more	Copy number loss	See cases	GPathogenic
Select item 145116	GRCh38/hg38 22q13.32-13.33(chr22:49003834-49601475)x3	LOC111828509, LOC126863181 +11 more	Copy number gain	See cases	GBenign
Select item 57704	GRCh38/hg38 22q13.33(chr22:49395349-50738932)x1	ACR, ADM2 +185 more	Copy number loss	See cases	GPathogenic
Select item 152142	GRCh38/hg38 22q13.33(chr22:49450335-49504768)x1	LOC129391290, MIR3667HG	Copy number loss	See cases	GBenign

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