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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3889596copy number variation1nstd102humanBenign GRCh37 chr2: 86,055,946-86,063,465 , GRCh38.p12 chr2: 85,828,823-85,836,342 ST3GAL5
    nsv3885717copy number variation1nstd102humanBenign GRCh37 chr2: 86,061,393-86,063,877 , GRCh38.p12 chr2: 85,834,270-85,836,754 ST3GAL5
    nsv3872857copy number variation1nstd102humanBenign GRCh37 chr2: 86,061,393-86,063,465 , GRCh38.p12 chr2: 85,834,270-85,836,342 ST3GAL5
    nsv3875535copy number variation1nstd102humanBenign GRCh37 chr2: 86,062,425-86,063,465 , GRCh38.p12 chr2: 85,835,302-85,836,342 ST3GAL5
    nsv3885385copy number variation1nstd102humanUncertain significance GRCh37 chr2: 86,067,247-86,116,048 , GRCh38 chr2: 85,840,124-85,888,925 ST3GAL5, ST3GAL5-AS1
    nsv4681626copy number variation1nstd102humanUncertain significance GRCh37 chr2: 86,115,927-86,116,048 , GRCh38.p12 chr2: 85,888,804-85,888,925 ST3GAL5, ST3GAL5-AS1
    nsv6311604copy number variation1nstd102humanUncertain significance GRCh37 chr2: 86,115,927-86,116,028 , GRCh38.p12 chr2: 85,888,804-85,888,905 ST3GAL5, ST3GAL5-AS1
    nsv6311526copy number variation1nstd102humanUncertain significance GRCh37 chr2: 86,067,267-86,332,899 , GRCh38.p12 chr2: 85,840,144-86,105,776 ST3GAL5, POLR1A, 3 more genes
    nsv3910630copy number variation1nstd102humanPathogenic 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 ST3GAL5, DAZAP2P1, 2991 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 ST3GAL5, CYP1B1-AS1, 1649 more genes
    nsv3877742copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,365,484-89,129,064 , GRCh38.p12 chr2: 74,138,357-88,829,551 ST3GAL5, RNU6-561P, 253 more genes
    nsv3886532copy number variation1nstd102humanPathogenic GRCh37 chr2: 74,527,522-89,125,488 , GRCh38.p12 chr2: 74,300,395-88,825,975 ST3GAL5, RNU6-561P, 249 more genes
    nsv4451607copy number variation1nstd102humanPathogenic GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842 ST3GAL5, REEP1, 134 more genes
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 ST3GAL5, VAMP8, 86 more genes
    nsv6313890copy number variation1nstd102humanPathogenic GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919 ST3GAL5, LOC105374836, 93 more genes
    nsv3899461copy number variation1nstd102humanPathogenic GRCh38 chr2: 85,014,686-88,826,619 , GRCh37 chr2: 85,241,809-89,126,132 , NCBI36 chr2: 85,095,320-88,907,247 ST3GAL5, CD8A, 115 more genes
    nsv7096524copy number variation1nstd102humanPathogenic GRCh37 chr2: 85,766,411-86,564,633 , GRCh38.p12 chr2: 85,539,288-86,337,510 ST3GAL5, GPR160P1, 27 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 ST3GAL5, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 ST3GAL5, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 ST3GAL5, RNU6-674P, 3735 more genes
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