Related gene-specific medical variations for Gene (Select 9904) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1807646	GRCh37/hg19 12q24.13-24.21(chr12:114251258-114555608)x3	RBM19	Copy number gain	not provided	GUncertain significance
Select item 980456	GRCh37/hg19 12q24.13-24.21(chr12:114264727-114556283)x3	RBM19	Copy number gain	not provided	GUncertain significance
Select item 442586	GRCh37/hg19 12q24.13-24.21(chr12:114103287-114656460)x3	RBM19	Copy number gain	See cases	GUncertain significance
Select item 394751	GRCh37/hg19 12q24.13-24.21(chr12:114277899-114548111)x3	RBM19	Copy number gain	See cases	GUncertain significance

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