Related gene-specific medical variations for Gene (Select 57144) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1340160	GRCh37/hg19 20p12.2(chr20:9537352-9808288)x3	PAK5	Copy number gain	not provided	GUncertain significance
Select item 689190	GRCh37/hg19 20p12.2(chr20:9736492-9881109)x3	PAK5	Copy number gain	not provided	GUncertain significance
Select item 688968	GRCh37/hg19 20p12.2(chr20:9736492-9886643)x3	PAK5	Copy number gain	not provided	GUncertain significance
Select item 687279	GRCh37/hg19 20p12.2(chr20:9736492-9886643)x3	PAK5	Copy number gain	not provided	GUncertain significance
Select item 685949	GRCh37/hg19 20p12.2(chr20:9736492-9886643)x4	PAK5	Copy number gain	not provided	GUncertain significance
Select item 685422	GRCh37/hg19 20p12.2(chr20:9736492-9881437)x3	PAK5	Copy number gain	not provided	GUncertain significance

ClinVar