"Ambry Genetics"[submitter] AND "MIR1915HG"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3126708	NR_160800.1(MIR1915HG):n.843G>C	MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2536824	NR_160800.1(MIR1915HG):n.798C>A	MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2536026	NR_160800.1(MIR1915HG):n.770C>G	MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3126707	NR_160800.1(MIR1915HG):n.753G>C	MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3294939	NR_160800.1(MIR1915HG):n.751C>G	MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3126706	NR_160800.1(MIR1915HG):n.750C>T	MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 3126705	NR_160800.1(MIR1915HG):n.742C>T	MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 2607419	NR_160800.1(MIR1915HG):n.738C>T	MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2523070	NR_160800.1(MIR1915HG):n.708C>T	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign
Select item 3126704	NR_160800.1(MIR1915HG):n.703T>G	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3126703	NR_160800.1(MIR1915HG):n.670C>A	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3126702	NR_160800.1(MIR1915HG):n.666G>A	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2493165	NR_160800.1(MIR1915HG):n.642C>G	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3126701	NR_160800.1(MIR1915HG):n.607A>T	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3126700	NR_160800.1(MIR1915HG):n.567G>A	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3126709	NR_160800.1(MIR1915HG):n.535G>A	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2490924	NR_160800.1(MIR1915HG):n.535G>C	LOC130003467, MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 2612849	NR_160800.1(MIR1915HG):n.490G>A	MIR1915HG	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance