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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5854813copy number variation1nstd209human GRCh38 chr13: 46,797,344-46,799,093 , GRCh37.p13 chr13: 47,371,479-47,373,228 ESD
    nsv5730317mobile element insertion1nstd211human GRCh38 chr13: 46,769,771-46,769,771 , GRCh37.p13 chr13: 47,343,906-47,343,906 ESD
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561330sequence alteration1nstd206human GRCh38 chr13: 44,983,377-49,709,767 , GRCh37.p13 chr13: 45,557,512-50,283,903 , ESD, 103 more genes
    nsv5159748mobile element insertion1nstd203human GRCh38 chr13: 46,785,213-46,785,223 , GRCh37.p13 chr13: 47,359,348-47,359,358 ESD
    nsv5004572copy number variation1nstd200human GRCh38 chr13: 46,563,331-47,747,867 , GRCh37.p13 chr13: 47,137,466-48,322,002 , LOC105370196, 8 more genes
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4834559copy number variation1nstd200human GRCh37 chr13: 47,137,466-48,322,002 , GRCh38.p12 chr13: 46,563,331-47,747,867 , HTR2A-AS1, 8 more genes
    nsv4728809copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 45,487,628-52,639,336 , GRCh38.p12 chr13: 44,913,493-52,065,200 ATP7B, RCBTB2, 155 more genes
    nsv4604503copy number variation1nstd183human GRCh37 chr13: 47,345,365-47,345,684 , GRCh38.p12 chr13: 46,771,230-46,771,549 ESD
    nsv4574905mobile element insertion1nstd166human GRCh37.p13 chr13: 47,371,355-47,371,355 , GRCh38.p12 chr13: 46,797,220-46,797,220 ESD
    nsv4509146mobile element insertion1nstd166human GRCh37.p13 chr13: 47,359,348-47,359,348 , GRCh38.p12 chr13: 46,785,213-46,785,213 ESD
    nsv4499977mobile element insertion1nstd166human GRCh37.p13 chr13: 47,361,539-47,361,539 , GRCh38.p12 chr13: 46,787,404-46,787,404 ESD
    nsv4457256copy number variation1nstd102humanUncertain significance GRCh37 chr13: 47,342,487-47,398,352 , GRCh38.p12 chr13: 46,768,352-46,824,217 ESD
    nsv4381419copy number variation1nstd173human GRCh37 chr13: 46,589,256-51,939,619 , GRCh38.p12 chr13: 46,015,121-51,365,483 , RNU6-68P, 105 more genes
    nsv4232281copy number variation1nstd166human GRCh37.p13 chr13: 47,137,466-48,322,002 , GRCh38.p12 chr13: 46,563,331-47,747,867 , LOC107984563, 8 more genes
    nsv4231125copy number variation1nstd166human GRCh37.p13 chr13: 47,345,668-47,345,805 , GRCh38.p12 chr13: 46,771,533-46,771,670 ESD
    nsv4228073copy number variation1nstd166human GRCh37.p13 chr13: 47,339,979-47,393,185 , GRCh38.p12 chr13: 46,765,844-46,819,050 ESD
    nsv3969901insertion1nstd168human GRCh38 chr13: 46,797,248-46,818,942 , GRCh37.p13 chr13: 47,371,383-47,393,077 ESD
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
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