Related gene-specific medical variations for Gene (Select 79741) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809381	GRCh37/hg19 10p11.22(chr10:32675281-32913940)x3	CCDC7	Copy number gain	not provided	GUncertain significance
Select item 1809376	GRCh37/hg19 10p11.22(chr10:32728348-32932673)x1	CCDC7	Copy number loss	not provided	GUncertain significance
Select item 815332	GRCh37/hg19 10p11.22(chr10:33041909-33124061)x1	CCDC7	Copy number loss	not provided	GUncertain significance
Select item 815331	GRCh37/hg19 10p11.22(chr10:32952403-33032845)x1	CCDC7	Copy number loss	not provided	GUncertain significance

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