Related gene-specific medical variations for Gene (Select 26260) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340645	GRCh37/hg19 8p23.3(chr8:234757-380770)x1	FBXO25	Copy number loss	not provided	GLikely benign
Select item 980865	GRCh37/hg19 8p23.3(chr8:237332-380770)x1	FBXO25	Copy number loss	not provided	GLikely benign
Select item 144393	GRCh38/hg38 8p23.3(chr8:410369-478189)x3	FBXO25	Copy number gain	See cases	GUncertain significance

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