Related gene-specific medical variations for Gene (Select 5218) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808626	GRCh37/hg19 7q21.13(chr7:90409326-90570411)x1	CDK14	Copy number loss	not provided	GUncertain significance
Select item 1340777	GRCh37/hg19 7q21.13(chr7:90350418-90405386)x1	CDK14	Copy number loss	not provided	GLikely benign
Select item 815008	GRCh37/hg19 7q21.13(chr7:90128713-90625015)x1	CDK14	Copy number loss	not provided	GUncertain significance
Select item 563274	GRCh37/hg19 7q21.13(chr7:90729485-90786957)x1	CDK14	Copy number loss	not provided	GUncertain significance

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