Related gene-specific medical variations for Gene (Select 286887) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3244446	NC_000012.11:g.(?_52863175)_(52863694_?)del	KRT6C	Deletion	not provided	GUncertain significance
Select item 687942	GRCh37/hg19 12q13.13(chr12:52864293-52880704)x1	KRT6C	Copy number loss	not provided	GUncertain significance
Select item 687679	GRCh37/hg19 12q13.13(chr12:52845923-52865918)x1	KRT6C	Copy number loss	not provided	GUncertain significance
Select item 687137	GRCh37/hg19 12q13.13(chr12:52845951-52865918)x1	KRT6C	Copy number loss	not provided	GUncertain significance
Select item 686158	GRCh37/hg19 12q13.13(chr12:52845951-52865918)x1	KRT6C	Copy number loss	not provided	GUncertain significance
Select item 685518	GRCh37/hg19 12q13.13(chr12:52845951-52865918)x1	KRT6C	Copy number loss	not provided	GUncertain significance
Select item 157253	NM_005555.3(KRT6B):c.-16752_-90del	KRT6C	Deletion	Normal pregnancy	Gnot provided

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