"GeneDx"[submitter] AND "EXOC3L2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2056980	NM_001382422.1(EXOC3L2):c.1741C>T (p.Arg581Cys)	EXOC3L2 (R581C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 253776	GRCh37/hg19 19q13.32(chr19:45284576-45978239)x3	NECTIN2, APOE +24 more	Copy number gain	See cases	GUncertain significance
Select item 253540	GRCh37/hg19 19q13.2-13.32(chr19:43013365-47241534)x1	APOC1, APOC2 +120 more	Copy number loss	See cases	GPathogenic

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