ranbp2[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
nsv4681044	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,336,043-109,357,157 , GRCh38.p12 chr2: 108,719,587-108,740,701	RANBP2
nsv6311284	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,363,147-109,368,470 , GRCh38.p12 chr2: 108,746,691-108,752,014	RANBP2
nsv6311149	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,367,700-109,368,470 , GRCh38.p12 chr2: 108,751,244-108,752,014	RANBP2
nsv5381326	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,356,925-109,357,157 , GRCh38.p12 chr2: 108,740,469-108,740,701	RANBP2
nsv6311334	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,347,210-109,392,412 , GRCh38.p12 chr2: 108,730,754-108,775,956	RANBP2
nsv6311148	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,363,147-109,370,447 , GRCh38.p12 chr2: 108,746,691-108,753,991	RANBP2
nsv7095848	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr2: 109,368,307-109,370,039 , GRCh38.p12 chr2: 108,751,851-108,753,583	RANBP2
nsv7096363	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,363,157-109,363,264 , GRCh38.p12 chr2: 108,746,701-108,746,808	RANBP2
nsv3889051	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 109,392,302-109,492,622 , GRCh38.p12 chr2: 108,775,846-108,876,166	RANBP2, CCDC138
nsv5564250	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,336,063-109,547,470 , GRCh38.p12 chr2: 108,719,607-108,931,014	RANBP2, EDAR, 2 more genes
nsv3881256	copy number variation	3	nstd102	human	Uncertain significance	GRCh37 chr2: 109,336,043-109,579,739 , GRCh38 chr2: 108,719,587-108,963,283	RANBP2, EDAR, 2 more genes
nsv5381336	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,336,063-109,579,739 , GRCh38.p12 chr2: 108,719,607-108,963,283	RANBP2, RPL39P16, 2 more genes
nsv4681091	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,345,568-109,579,739 , GRCh38.p12 chr2: 108,729,112-108,963,283	RANBP2, RPL39P16, 2 more genes
nsv4450149	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr2: 108,751,508-108,963,283 , GRCh37 chr2: 109,367,964-109,579,739	RANBP2, CCDC138, 2 more genes
nsv7096323	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 109,368,307-109,579,739 , GRCh38.p12 chr2: 108,751,851-108,963,283	RANBP2, CCDC138, 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	RANBP2, 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	RANBP2, CYP1B1-AS1, 1649 more genes
nsv3872550	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 106,423,310-115,054,828 , GRCh38.p12 chr2: 105,806,853-114,297,251	RANBP2, SMIM12P1, 189 more genes
nsv4728410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 107,029,680-113,187,742 , GRCh38.p12 chr2: 106,413,224-112,430,165	RANBP2, RPL10P5, 121 more genes
nsv6313505	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 108,446,955-110,504,318 , GRCh38.p12 chr2: 107,830,499-109,746,741	RANBP2, SULT1C3, 37 more genes

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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 57

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Number of Variants: 20

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Supplemental Content

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