LINC02820[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	ACAD10, ACADS +4836 more	Copy number gain	See cases	GPathogenic
Select item 155032	GRCh38/hg38 12q21.1-22(chr12:73485697-92795805)x1	ACSS3, ALX1 +287 more	Copy number loss	See cases	GPathogenic
Select item 59816	GRCh38/hg38 12q21.2-21.31(chr12:77564757-85370822)x3	ACSS3, ALX1 +66 more	Copy number gain	See cases	GPathogenic
Select item 148242	GRCh38/hg38 12q21.31(chr12:85228467-85675435)x1	ALX1, LINC02820 +8 more	Copy number loss	See cases	GUncertain significance
Select item 147411	GRCh38/hg38 12q21.31(chr12:85253355-85319830)x1	ALX1, LINC02820 +3 more	Copy number loss	See cases	GUncertain significance

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