RNU1-3[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2664871	GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3	A2ML1-AS2, A3GALT2 +2151 more	Copy number gain	Trisomy 12p	GPathogenic
Select item 59846	GRCh38/hg38 1p36.32-36.13(chr1:3006193-17688934)x1	LINC02783, LINC03126 +804 more	Copy number loss	See cases	GPathogenic
Select item 154704	GRCh38/hg38 1p36.31-36.13(chr1:5363826-18360302)x1	PLOD1, PRAMEF1 +730 more	Copy number loss	See cases	GPathogenic
Select item 58056	GRCh38/hg38 1p36.21-36.13(chr1:13619979-18466172)x3	LOC129929515, LOC129929516 +211 more	Copy number gain	See cases	GPathogenic
Select item 57443	GRCh38/hg38 1p36.21-36.12(chr1:15385267-20980349)x1	ACTL8, AGMAT +303 more	Copy number loss	See cases	GPathogenic
Select item 149010	GRCh38/hg38 1p36.21-36.13(chr1:15681812-19662339)x1	LOC126805640, LOC126805641 +206 more	Copy number loss	See cases	GPathogenic
Select item 147616	GRCh38/hg38 1p36.13(chr1:16487877-16778041)x1	FAM231AP, LINC01783 +14 more	Copy number loss	See cases	GBenign
Select item 147615	GRCh38/hg38 1p36.13(chr1:16487877-16778041)x3	FAM231AP, LINC01783 +14 more	Copy number gain	See cases	GBenign
Select item 146992	GRCh38/hg38 1p36.13(chr1:16600282-16722267)x1	FAM231AP, LOC129929532 +5 more	Copy number loss	See cases	GBenign
Select item 150893	GRCh38/hg38 1p36.13(chr1:16600450-16856300)x3	FAM231AP, LOC129929532 +8 more	Copy number gain	See cases	GLikely benign
Select item 150162	GRCh38/hg38 1p36.13(chr1:16600450-16761944)x3	FAM231AP, LOC129929532 +7 more	Copy number gain	See cases	GLikely benign
Select item 146668	GRCh38/hg38 1p36.13(chr1:16615158-16905322)x3	FAM231AP, LINC03126 +17 more	Copy number gain	See cases	GBenign
Select item 146654	GRCh38/hg38 1p36.13(chr1:16621632-16905322)x1	FAM231AP, LINC03126 +17 more	Copy number loss	See cases	GBenign
Select item 147294	GRCh38/hg38 1p36.13(chr1:16637078-16727421)x1	FAM231AP, LOC129929533 +4 more	Copy number loss	See cases	GBenign