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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945844copy number variation1nstd209human GRCh38 chr13: 52,141,931-52,143,159 , GRCh37.p13 chr13: 52,716,067-52,717,295 NEK3
    nsv5856130copy number variation1nstd209human GRCh38 chr13: 52,141,965-52,143,564 , GRCh37.p13 chr13: 52,716,101-52,717,700 NEK3
    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
    nsv5006485copy number variation1nstd200human GRCh38 chr13: 52,151,699-52,151,789 , GRCh37.p13 chr13: 52,725,834-52,725,924 NEK3
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4840861copy number variation1nstd200human GRCh37 chr13: 52,725,835-52,725,924 , GRCh38.p12 chr13: 52,151,700-52,151,789 NEK3
    nsv4769378copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,170,957-57,713,087 , GRCh38.p12 chr13: 51,596,821-57,138,953 CTAGE3P, TMEM272, 46 more genes
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv4457243copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,505,074-52,763,413 , GRCh38.p12 chr13: 51,930,938-52,189,278 UTP14C, NEK5, 7 more genes
    nsv4456820copy number variation1nstd102humanUncertain significance GRCh37 chr13: 49,586,017-61,311,845 , GRCh38.p12 chr13: 49,011,881-60,737,711 MIR759, CAB39L, 149 more genes
    nsv4456090copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,538,548-53,354,011 , GRCh38.p12 chr13: 51,964,412-52,779,876 FABP5P2, VPS36, 19 more genes
    nsv4386901copy number variation1nstd173human GRCh37 chr13: 52,621,073-52,775,838 , GRCh38.p12 chr13: 52,046,937-52,201,703 NEK5, MRPS31P5, 3 more genes
    nsv4386353copy number variation1nstd173human GRCh37 chr13: 52,620,824-52,775,838 , GRCh38.p12 chr13: 52,046,688-52,201,703 NEK3, NEK5, 3 more genes
    nsv4383300copy number variation1nstd173human GRCh37 chr13: 52,448,537-52,809,875 , GRCh38.p12 chr13: 51,874,401-52,235,740 FABP5P2, ALG11, 9 more genes
    nsv4223199copy number variation1nstd166human GRCh37.p13 chr13: 52,725,835-52,725,924 , GRCh38.p12 chr13: 52,151,700-52,151,789 NEK3
    nsv3960093insertion1nstd168human GRCh38 chr13: 52,096,310-52,131,783 , GRCh37.p13 chr13: 52,670,446-52,705,919 NEK3, NEK5, 1 more genes
    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
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3924052copy number variation1nstd102humanPathogenic GRCh38 chr13: 41,288,493-85,137,552 , NCBI36 chr13: 40,760,629-84,609,688 , GRCh37 chr13: 41,862,629-85,711,687 TMEM272, LOC105370241, 535 more genes
    nsv3923911copy number variation1nstd102humanPathogenic GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921 MLNR, SIAH3, 422 more genes
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