MIR4307HG[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59932	GRCh38/hg38 14q11.2-21.1(chr14:20000611-38984415)x3	LOC130055392, LOC130055393 +780 more	Copy number gain	See cases	GPathogenic
Select item 155119	GRCh38/hg38 14q11.2-21.2(chr14:20022693-44093672)x3	ABHD4, ACIN1 +814 more	Copy number gain	See cases	GPathogenic
Select item 155681	GRCh38/hg38 14q11.2-21.3(chr14:20043513-48642042)x3	OR10G2, OR10G3 +859 more	Copy number gain	See cases	GPathogenic
Select item 155306	GRCh38/hg38 14q11.2-32.33(chr14:20043514-106877229)x3	LOC126862060, LOC126862061 +3282 more	Copy number gain	See cases	GPathogenic
Select item 146230	GRCh38/hg38 14q11.2-32.33(chr14:20151149-106855263)x3	LOC125048449, LOC125048450 +3277 more	Copy number gain	See cases	GPathogenic
Select item 57745	GRCh38/hg38 14q11.2-21.2(chr14:20196945-45284802)x1	LOC112214170, LOC112214171 +840 more	Copy number loss	See cases	GPathogenic
Select item 57750	GRCh38/hg38 14q11.2-21.1(chr14:23548960-41983402)x1	MIR4503, MIR624 +399 more	Copy number loss	See cases	GPathogenic
Select item 153258	GRCh38/hg38 14q12(chr14:26355822-26905434)x3	LINC02293, LINC02294 +4 more	Copy number gain	See cases	GUncertain significance
Select item 146627	GRCh38/hg38 14q12(chr14:26599780-27710714)x1	LINC00645, LINC02293 +7 more	Copy number loss	See cases	GBenign
Select item 152352	GRCh38/hg38 14q12(chr14:26741728-27322789)x1	LINC02293, LINC02294 +5 more	Copy number loss	See cases	GLikely benign
Select item 149156	GRCh38/hg38 14q12(chr14:26905754-27478931)x1	MIR3171HG, MIR4307 +1 more	Copy number loss	See cases	GUncertain significance