Related gene-specific medical variations for Gene (Select 497634) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 443009	GRCh37/hg19 8q11.1-11.21(chr8:47597933-48172962)x3	LINC00293	Copy number gain	See cases	GUncertain significance
Select item 441936	GRCh37/hg19 8q11.1(chr8:47163897-48099109)x3	LINC00293	Copy number gain	See cases	GLikely benign
Select item 393840	GRCh37/hg19 8q11.1(chr8:47677629-47766983)x1	LINC00293	Copy number loss	See cases	GLikely benign

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