xpo1[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3903489	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr2: 61,369,298-61,576,198 , GRCh37 chr2: 61,515,794-61,722,694 , GRCh38 chr2: 61,288,659-61,495,559	XPO1, USP34, 2 more genes
nsv3887813	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 61,566,536-61,803,309 , GRCh38.p12 chr2: 61,339,401-61,576,174	XPO1, SNORA70B, 3 more genes
nsv3870645	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 61,605,123-61,786,583 , GRCh38.p12 chr2: 61,377,988-61,559,448	XPO1, USP34-DT, 2 more genes
nsv4454322	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 61,511,303-61,743,842 , GRCh38.p12 chr2: 61,284,168-61,516,707	XPO1, USP34-DT, 2 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	XPO1, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	XPO1, CYP1B1-AS1, 1649 more genes
nsv3892726	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 56,818,693-62,554,307 , GRCh38 chr2: 56,738,054-62,473,668 , GRCh37 chr2: 56,965,189-62,700,803	XPO1, RPS29P10, 66 more genes
nsv3903187	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 58,112,555-63,692,448 , GRCh38 chr2: 58,031,916-63,611,810 , GRCh37 chr2: 58,259,051-63,838,944	XPO1, RPL31P30, 76 more genes
nsv3904784	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 58,953,678-64,270,970 , GRCh37 chr2: 59,100,174-64,417,466 , GRCh38 chr2: 58,873,039-64,190,332	XPO1, UGP2, 79 more genes
nsv3891231	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 57,249,378-61,842,734 , NCBI36 chr2: 57,330,017-61,923,373 , GRCh37 chr2: 57,476,513-62,069,869	XPO1, SANBR, 52 more genes
nsv3902458	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 59,885,981-62,563,218 , NCBI36 chr2: 59,739,485-62,416,722 , GRCh38 chr2: 59,658,846-62,336,083	XPO1, MIR4432, 48 more genes
nsv3891542	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 59,305,637-61,702,349 , GRCh38 chr2: 59,224,998-61,621,710 , GRCh37 chr2: 59,452,133-61,848,845	XPO1, SANBR, 36 more genes
nsv3898402	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 61,596,077-62,386,487 , GRCh38 chr2: 61,515,438-62,305,848 , GRCh37 chr2: 61,742,573-62,532,983	XPO1, LOC100533678, 17 more genes
nsv6636439	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 61,379,352-61,928,100 , GRCh38.p12 chr2: 61,152,217-61,700,965	XPO1, C2orf74, 8 more genes
nsv6636424	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 61,215,497-61,714,418 , GRCh38.p12 chr2: 60,988,362-61,487,283	XPO1, PUS10, 11 more genes
nsv997086	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr2: 58,912,065-62,261,736 , GRCh37 chr2: 59,139,200-62,488,871	XPO1, ATP1B3P1, 52 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	XPO1, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	XPO1, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	XPO1, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	XPO1, MTND2P22, 3724 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 39

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Number of Variants: 20

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