MIR1915HG[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 149407	GRCh38/hg38 10p15.3-12.1(chr10:90205-26339978)x3	ACBD7, ACBD7-DCLRE1CP1 +837 more	Copy number gain	See cases	GPathogenic
Select item 152998	GRCh38/hg38 10p15.1-q11.22(chr10:4604734-48074662)x3	ABI1, ACBD5 +1221 more	Copy number gain	See cases	GBenign
Select item 148232	GRCh38/hg38 10p14-12.31(chr10:7428770-21587752)x1	ACBD7, ACBD7-DCLRE1CP1 +388 more	Copy number loss	See cases	GPathogenic
Select item 150600	GRCh38/hg38 10p12.31-11.22(chr10:19088161-32732293)x3	ABI1, ACBD5 +376 more	Copy number gain	See cases	GLikely pathogenic
Select item 150847	GRCh38/hg38 10p12.31(chr10:20964970-22049554)x3	C10orf113, DNAJC1 +35 more	Copy number gain	See cases	GUncertain significance
Select item 146066	GRCh38/hg38 10p12.31(chr10:21125825-21721227)x3	C10orf113, LINC02643 +20 more	Copy number gain	See cases	GUncertain significance
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
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	AGAP5, CRTAC1 +682 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574686	GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	ABRAXAS2, CHCHD1 +673 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 1527577	GRCh37/hg19 10p15.1-11.21(chr10:6273934-34732521)	ABI1, ACBD5 +111 more	Copy number gain	not specified	GPathogenic
Select item 1339781	GRCh37/hg19 10p15.3-q11.22(chr10:135655-47688677)x4	ARL5B, LARP4B +180 more	Copy number gain	Mosaic supernumerary isodicentric chromosome 10	Gnot provided
Select item 686574	GRCh37/hg19 10p12.31(chr10:19774176-22330966)x1	C10orf113, DNAJC1 +6 more	Copy number loss	not provided	GUncertain significance
Select item 443260	GRCh37/hg19 10p15.3-q11.23(chr10:100026-50961640)x3	ABI1, ACBD5 +205 more	Copy number gain	See cases	GPathogenic
Select item 441987	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)	INA, INPP5A +721 more	Copy number gain	See cases	GPathogenic
Select item 441986	GRCh37/hg19 10p15.3-q26.3(chr10:100027-135427143)x3	A1CF, ABCC2 +721 more	Copy number gain	See cases	GPathogenic
Select item 393995	GRCh37/hg19 10p15.3-q26.3(chr10:93297-135378918)x3	A1CF, ABCC2 +722 more	Copy number gain	See cases	GPathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 33