MIR4300HG[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144356	GRCh38/hg38 11q13.5-22.1(chr11:75941754-98357960)x1	AAMDC, ACER3 +474 more	Copy number loss	See cases	GPathogenic
Select item 58918	GRCh38/hg38 11q14.1-22.3(chr11:78232836-106779420)x1	LINC02553, LINC02700 +528 more	Copy number loss	See cases	GPathogenic
Select item 59771	GRCh38/hg38 11q14.1-14.2(chr11:78362208-86165380)x3	ANKRD42, ANKRD42-DT +117 more	Copy number gain	See cases	GPathogenic
Select item 150225	GRCh38/hg38 11q14.1(chr11:80281651-82521009)x1	LINC02720, LOC126861278 +5 more	Copy number loss	See cases	GUncertain significance
Select item 146269	GRCh38/hg38 11q14.1(chr11:81686030-82113389)x1	LOC126861278, LOC130006514 +2 more	Copy number loss	See cases	GUncertain significance

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