ClinVar for Gene (Select 130005221) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 153246	GRCh38/hg38 11p15.4(chr11:7359664-7657396)x1	LOC113939928, LOC124902806 +25 more	Copy number loss	See cases	GUncertain significance
Select item 151263	GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3	DENND5A, DNHD1 +723 more	Copy number gain	See cases	GPathogenic
Select item 150272	GRCh38/hg38 11p15.4(chr11:7187414-7707594)x3	CYB5R2, LOC113939928 +34 more	Copy number gain	See cases	GUncertain significance
Select item 144515	GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3	TRIM22, TRIM3 +917 more	Copy number gain	See cases	GPathogenic

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