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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5704598mobile element insertion2nstd211human GRCh38 chr10: 125,766,505-125,766,505 , GRCh37.p13 chr10: 127,455,074-127,455,074 MMP21
    nsv5494334copy number variation1nstd206human GRCh38 chr10: 125,766,224-125,766,517 , GRCh37.p13 chr10: 127,454,793-127,455,086 MMP21
    nsv5405004mobile element insertion1nstd206human GRCh38 chr10: 125,766,505-125,766,556 , GRCh37.p13 chr10: 127,455,074-127,455,125 MMP21
    nsv5133869mobile element insertion1nstd203human GRCh38 chr10: 125,766,491-125,766,505 , GRCh37.p13 chr10: 127,455,060-127,455,074 MMP21
    nsv4983971copy number variation1nstd200human GRCh38 chr10: 125,039,754-126,334,238 , GRCh37.p13 chr10: 126,728,323-128,022,807 , ADAM12, 28 more genes
    nsv4977433copy number variation1nstd200human GRCh38 chr10: 125,772,633-125,772,693 , GRCh37.p13 chr10: 127,461,202-127,461,262 MMP21
    nsv4977432copy number variation1nstd200human GRCh38 chr10: 125,772,332-125,778,257 , GRCh37.p13 chr10: 127,460,901-127,466,826 MMP21
    nsv4846440copy number variation1nstd200human GRCh37 chr10: 127,454,793-127,455,086 , GRCh38.p12 chr10: 125,766,224-125,766,517 MMP21
    nsv4838226copy number variation1nstd200human GRCh37 chr10: 127,461,202-127,461,262 , GRCh38.p12 chr10: 125,772,633-125,772,693 MMP21
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4610879copy number variation1nstd183human GRCh37 chr10: 127,459,480-127,491,165 , GRCh38.p12 chr10: 125,770,911-125,802,596 MMP21, UROS
    nsv4481820mobile element insertion1nstd166human GRCh37.p13 chr10: 127,455,060-127,455,060 , GRCh38.p12 chr10: 125,766,491-125,766,491 MMP21
    nsv4456733copy number variation1nstd102humanPathogenic GRCh37 chr10: 124,988,334-135,427,143 , GRCh38.p12 chr10: 123,228,818-133,613,639 FAM53B-AS1, LOC105378544, 153 more genes
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
    nsv4196040copy number variation1nstd166human GRCh37.p13 chr10: 127,454,793-127,455,086 , GRCh38.p12 chr10: 125,766,224-125,766,517 MMP21
    nsv3924720copy number variation1nstd102humanPathogenic GRCh38 chr10: 119,707,856-133,613,639 , GRCh37 chr10: 121,467,368-135,427,143 , NCBI36 chr10: 121,457,358-135,277,133 OR6L2P, RPL19P16, 208 more genes
    nsv3923859copy number variation1nstd102humanPathogenic NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674 AS-PTPRE, SFXN4, 330 more genes
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