vamp8[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
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	VAMP8, 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	VAMP8, CYP1B1-AS1, 1649 more genes
nsv3877742	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551	VAMP8, RNU6-561P, 253 more genes
nsv3886532	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975	VAMP8, RNU6-561P, 249 more genes
nsv4451607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842	VAMP8, REEP1, 134 more genes
nsv6112750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907	VAMP8, TMSB10, 86 more genes
nsv6313890	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919	VAMP8, LOC105374836, 93 more genes
nsv3899461	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 85,014,686-88,826,619 , GRCh37 chr2: 85,241,809-89,126,132 , NCBI36 chr2: 85,095,320-88,907,247	VAMP8, CD8A, 115 more genes
nsv7096524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 85,766,411-86,564,633 , GRCh38.p12 chr2: 85,539,288-86,337,510	VAMP8, GPR160P1, 27 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	VAMP8, 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	VAMP8, 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	VAMP8, 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	VAMP8, MTND2P22, 3724 more genes
nsv3916821	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722	VAMP8, NAGK, 595 more genes
nsv3897079	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 77,025,216-90,282,666 , NCBI36 chr2: 77,105,850-90,982,989 , GRCh37 chr2: 77,252,342-91,619,262	VAMP8, IGKV2D-18, 280 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	VAMP8, ACTG2, 1713 more genes
nsv3903805	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899	VAMP8, LOC101927723, 1246 more genes
nsv3882844	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 82,517,612-86,262,705 , GRCh38.p12 chr2: 82,290,488-86,035,582	VAMP8, TMEM150A, 69 more genes
nsv4728539	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 85,786,006-86,559,358 , GRCh38.p12 chr2: 85,558,883-86,332,235	VAMP8, ST3GAL5-AS1, 25 more genes
nsv6636862	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 85,786,007-86,559,358 , GRCh38.p12 chr2: 85,558,884-86,332,235	VAMP8, MIR4779, 25 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 21

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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