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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5857094copy number variation1nstd209human GRCh38 chr12: 112,907,468-112,909,767 , GRCh37.p13 chr12: 113,345,273-113,347,572 OAS1
    nsv5707171mobile element insertion1nstd211human GRCh38 chr12: 112,906,937-112,906,937 , GRCh37.p13 chr12: 113,344,742-113,344,742 OAS1
    nsv5496430copy number variation1nstd206human GRCh38 chr12: 112,909,434-112,910,261 , GRCh37.p13 chr12: 113,347,239-113,348,066 OAS1
    nsv5417049mobile element insertion1nstd206human GRCh38 chr12: 112,906,937-112,906,980 , GRCh37.p13 chr12: 113,344,742-113,344,785 OAS1
    nsv4995681copy number variation1nstd200human GRCh38 chr12: 112,913,511-112,913,573 , GRCh37.p13 chr12: 113,351,316-113,351,378 OAS1
    nsv4995680copy number variation1nstd200human GRCh38 chr12: 112,909,434-112,910,261 , GRCh37.p13 chr12: 113,347,239-113,348,066 OAS1
    nsv4832401copy number variation1nstd200human GRCh37 chr12: 113,347,233-113,348,066 , GRCh38.p12 chr12: 112,909,428-112,910,261 OAS1
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4603423copy number variation1nstd183human GRCh37 chr12: 113,360,558-113,367,311 , GRCh38.p12 chr12: 112,922,753-112,929,506 OAS1
    nsv4601004copy number variation1nstd183human GRCh37 chr12: 113,355,252-113,438,258 , GRCh38.p12 chr12: 112,917,447-113,000,453 OAS2, OAS1, 1 more genes
    nsv4231372copy number variation1nstd166human GRCh37.p13 chr12: 113,343,599-113,385,319 , GRCh38.p12 chr12: 112,905,794-112,947,514 OAS3, OAS1
    nsv4217735copy number variation1nstd166human GRCh37.p13 chr12: 113,358,054-113,358,107 , GRCh38.p12 chr12: 112,920,249-112,920,302 OAS1
    nsv4217647copy number variation1nstd166human GRCh37.p13 chr12: 113,347,239-113,348,066 , GRCh38.p12 chr12: 112,909,434-112,910,261 OAS1
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 , OR5BT1P, 2441 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 , RNA5SP369, 2454 more genes
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