"GeneDx"[submitter] AND "MIR4649"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59680	GRCh38/hg38 7p14.3-q11.21(chr7:33328312-62377476)x3	LOC129389795, LOC129389796 +636 more	Copy number gain	See cases	GPathogenic
Select item 59304	GRCh38/hg38 7p14.1-12.3(chr7:39814159-45749735)x1	SNORA5A, SNORA5B +212 more	Copy number loss	See cases	GPathogenic
Select item 709786	NM_001129.5(AEBP1):c.1486-8C>G	AEBP1, MIR4649	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign/Likely benign

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