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Items: 1 to 20 of 1218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5948895insertion1nstd209human GRCh38 chr2: 239,345,395-239,345,395 , GRCh37.p13 chr2: 240,267,090-240,267,090 HDAC4
    nsv5905817copy number variation1nstd209human GRCh38 chr2: 239,292,655-239,294,758 , GRCh37.p13 chr2: 240,214,350-240,216,453 HDAC4
    nsv5905297copy number variation1nstd209human GRCh38 chr2: 239,360,661-239,360,713 , GRCh37.p13 chr2: 240,282,356-240,282,408 HDAC4
    nsv5904451copy number variation1nstd209human GRCh38 chr2: 239,280,955-239,281,207 , GRCh37.p13 chr2: 240,202,651-240,202,903 HDAC4
    nsv5901924copy number variation1nstd209human GRCh38 chr2: 239,119,911-239,119,981 , GRCh37.p13 chr2: 240,041,607-240,041,677 HDAC4
    nsv5900997copy number variation1nstd209human GRCh38 chr2: 239,143,481-239,143,579 , GRCh37.p13 chr2: 240,065,177-240,065,275 HDAC4
    nsv5900996copy number variation1nstd209human GRCh38 chr2: 239,317,863-239,317,953 , GRCh37.p13 chr2: 240,239,558-240,239,648 HDAC4
    nsv5900710copy number variation1nstd209human GRCh38 chr2: 239,075,964-239,076,028 , GRCh37.p13 chr2: 239,997,660-239,997,724 HDAC4
    nsv5900090copy number variation1nstd209human GRCh38 chr2: 239,150,865-239,150,919 , GRCh37.p13 chr2: 240,072,561-240,072,615 HDAC4
    nsv5899125copy number variation1nstd209human GRCh38 chr2: 239,119,517-239,120,104 , GRCh37.p13 chr2: 240,041,213-240,041,800 HDAC4
    nsv5899036copy number variation1nstd209human GRCh38 chr2: 239,347,005-239,347,090 , GRCh37.p13 chr2: 240,268,700-240,268,785 HDAC4
    nsv5898236copy number variation1nstd209human GRCh38 chr2: 239,094,385-239,094,443 , GRCh37.p13 chr2: 240,016,081-240,016,139 HDAC4
    nsv5897640copy number variation1nstd209human GRCh38 chr2: 239,084,671-239,084,756 , GRCh37.p13 chr2: 240,006,367-240,006,452 HDAC4, MIR4441
    nsv5896959copy number variation1nstd209human GRCh38 chr2: 239,366,783-239,367,056 , GRCh37.p13 chr2: 240,288,478-240,288,751 HDAC4
    nsv5896385copy number variation1nstd209human GRCh38 chr2: 239,280,970-239,281,333 , GRCh37.p13 chr2: 240,202,666-240,203,029 HDAC4
    nsv5895549copy number variation1nstd209human GRCh38 chr2: 239,269,164-239,269,231 , GRCh37.p13 chr2: 240,190,860-240,190,927 HDAC4
    nsv5894939copy number variation1nstd209human GRCh38 chr2: 239,124,588-239,124,647 , GRCh37.p13 chr2: 240,046,284-240,046,343 HDAC4
    nsv5893924copy number variation1nstd209human GRCh38 chr2: 239,112,958-239,113,442 , GRCh37.p13 chr2: 240,034,654-240,035,138 HDAC4
    nsv5891867copy number variation1nstd209human GRCh38 chr2: 239,068,891-239,069,585 , GRCh37.p13 chr2: 239,990,587-239,991,281 MIR4440, HDAC4
    nsv5890843copy number variation1nstd209human GRCh38 chr2: 239,169,766-239,169,818 , GRCh37.p13 chr2: 240,091,462-240,091,514 HDAC4
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