Related gene-specific medical variations for Gene (Select 64881) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685469	GRCh37/hg19 13q21.2-21.32(chr13:61460314-66500456)x1	PCDH20	Copy number loss	not provided	GUncertain significance
Select item 979375	GRCh37/hg19 13q21.2-21.31(chr13:61660181-63785757)x3	PCDH20	Copy number gain	not provided	GLikely benign
Select item 443642	GRCh37/hg19 13q21.2-21.31(chr13:61660181-63785757)x3	PCDH20	Copy number gain	See cases	Gconflicting data from submitters

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