"GeneDx"[submitter] AND "MTHFD2L"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58029	GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3	LOC129389216, LOC129389217 +757 more	Copy number gain	See cases	GPathogenic
Select item 58031	GRCh38/hg38 4q13.3-21.21(chr4:71128874-78099088)x3	ADAMTS3, AFM +166 more	Copy number gain	See cases	GPathogenic
Select item 151069	GRCh38/hg38 4q13.3(chr4:74173208-74240861)x1	LOC112978671, LOC129992675 +1 more	Copy number loss	See cases	GUncertain significance

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