729911[Gene ID] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057816, LOC130057817 +1763 more	Copy number gain	See cases	GPathogenic
Select item 154952	GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3	ABHD17C, ABHD2 +1244 more	Copy number gain	See cases	GPathogenic
Select item 147979	GRCh38/hg38 15q24.2-25.1(chr15:76006154-79982417)x1	ACSBG1, ADAMTS7 +175 more	Copy number loss	See cases	GPathogenic
Select item 1249129	NC_000015.10:g.79209525T>G	ANKRD34C-AS1, MIR184	Single nucleotide variant	not provided	GBenign
Select item 1223338	NC_000015.10:g.79209754G>C	ANKRD34C-AS1, MIR184	Single nucleotide variant	not provided	GBenign
Select item 1219828	NC_000015.10:g.79209778T>C	ANKRD34C-AS1, MIR184	Single nucleotide variant	not provided	GLikely benign
Select item 1606846	NR_029705.1(MIR184):n.39G>T	ANKRD34C-AS1, MIR184	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1065584	NR_029705.1(MIR184):n.52T>C	ANKRD34C-AS1, MIR184	Single nucleotide variant (non-coding transcript variant)	MIR184-related condition	GUncertain significance
Select item 3011947	NR_029705.1(MIR184):n.55G>A	ANKRD34C-AS1, MIR184	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 31007	NR_029705.1(MIR184):n.57C>T	ANKRD34C-AS1, MIR184	Single nucleotide variant (non-coding transcript variant)	EDICT syndrome	GPathogenic
Select item 1175607	NC_000015.10:g.79209980T>C	ANKRD34C-AS1, MIR184	Single nucleotide variant	not provided	GBenign
Select item 1246314	NC_000015.10:g.79210027G>C	MIR184, ANKRD34C-AS1	Single nucleotide variant	not provided	GBenign