"GeneDx"[submitter] AND "LOC126806069"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58116	GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3	LOC120908923, LOC120947224 +1352 more	Copy number gain	See cases	GPathogenic
Select item 60117	GRCh38/hg38 1q43-44(chr1:237906379-244022201)x1	AKT3, AKT3-IT1 +55 more	Copy number loss	See cases	GPathogenic
Select item 2579619	NM_020066.5(FMN2):c.4150C>T (p.His1384Tyr)	FMN2, LOC126806069 (H1384Y +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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