Related gene-specific medical variations for Gene (Select 5890) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1527824	GRCh37/hg19 14q24.1(chr14:68448694-68854357)	RAD51B	Copy number gain	not specified	GUncertain significance
Select item 1340745	GRCh37/hg19 14q24.1(chr14:68341429-68567227)x1	RAD51B	Copy number loss	not provided	GUncertain significance
Select item 442442	GRCh37/hg19 14q24.1(chr14:68423442-68895183)x1	RAD51B	Copy number loss	See cases	GUncertain significance
Select item 162174	NM_133510.4(RAD51B):c.853+26380G>A	RAD51B	Single nucleotide variant (intron variant)	not provided	Gnot provided

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