LOC101928985[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59772	GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3	AASDHPPT, ABCG4 +1199 more	Copy number gain	See cases	GPathogenic
Select item 148508	GRCh38/hg38 11q23.2-25(chr11:112864326-131189315)x3	BCL9L, BLID +774 more	Copy number gain	See cases	GPathogenic
Select item 57036	GRCh38/hg38 11q23.2-23.3(chr11:113444446-120648921)x3	LOC130006895, LOC130006896 +355 more	Copy number gain	See cases	GPathogenic
Select item 58188	GRCh38/hg38 11q23.3(chr11:115159099-116045030)x3	CADM1, CADM1-AS1 +19 more	Copy number gain	See cases	GUncertain significance
Select item 147770	GRCh38/hg38 11q23.3(chr11:115463428-115770089)x3	CADM1, LINC00900 +5 more	Copy number gain	See cases	GUncertain significance
Select item 148511	GRCh38/hg38 11q23.3(chr11:115647670-117581883)x3	APOA1, APOA1-AS +83 more	Copy number gain	See cases	GUncertain significance

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