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Items: 1 to 20 of 1047

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966380insertion1nstd209human GRCh38 chr2: 99,820,748-99,820,748 , GRCh37.p13 chr2: 100,437,210-100,437,210 , AFF3
    nsv5958523insertion1nstd209human GRCh38 chr2: 100,104,798-100,104,798 , GRCh37.p13 chr2: 100,721,260-100,721,260 AFF3
    nsv5948919insertion1nstd209human GRCh38 chr2: 99,724,271-99,724,271 , GRCh37.p13 chr2: 100,340,733-100,340,733 AFF3
    nsv5884366copy number variation1nstd209human GRCh38 chr2: 99,715,853-99,718,884 , GRCh37.p13 chr2: 100,332,315-100,335,346 AFF3
    nsv5880179copy number variation1nstd209human GRCh38 chr2: 99,736,670-99,739,655 , GRCh37.p13 chr2: 100,353,132-100,356,117 AFF3
    nsv5875504copy number variation1nstd209human GRCh38 chr2: 99,590,758-99,592,698 , GRCh37.p13 chr2: 100,207,220-100,209,160 AFF3
    nsv5870062copy number variation1nstd209human GRCh38 chr2: 99,776,227-99,808,014 , GRCh37.p13 chr2: 100,392,689-100,424,476 AFF3
    nsv5869667copy number variation1nstd209human GRCh38 chr2: 99,901,885-99,908,374 , GRCh37.p13 chr2: 100,518,347-100,524,836 AFF3
    nsv5869352copy number variation1nstd209human GRCh38 chr2: 99,631,955-99,633,166 , GRCh37.p13 chr2: 100,248,417-100,249,628 AFF3
    nsv5834172copy number variation1nstd209human GRCh38 chr2: 99,901,845-99,908,325 , GRCh37.p13 chr2: 100,518,307-100,524,787 AFF3
    nsv5834171copy number variation1nstd209human GRCh38 chr2: 99,849,507-99,850,506 , GRCh37.p13 chr2: 100,465,969-100,466,968 AFF3
    nsv5834170copy number variation1nstd209human GRCh38 chr2: 99,781,349-99,783,598 , GRCh37.p13 chr2: 100,397,811-100,400,060 AFF3
    nsv5834169copy number variation1nstd209human GRCh38 chr2: 99,736,634-99,739,633 , GRCh37.p13 chr2: 100,353,096-100,356,095 AFF3
    nsv5834168copy number variation1nstd209human GRCh38 chr2: 99,716,064-99,718,924 , GRCh37.p13 chr2: 100,332,526-100,335,386 AFF3
    nsv5834167copy number variation1nstd209human GRCh38 chr2: 99,590,739-99,592,638 , GRCh37.p13 chr2: 100,207,201-100,209,100 AFF3
    nsv5833892copy number variation1nstd209human GRCh38 chr2: 99,775,937-99,803,132 , GRCh37.p13 chr2: 100,392,399-100,419,594 AFF3
    nsv5722651mobile element insertion2nstd211human GRCh38 chr2: 99,760,325-99,760,325 , GRCh37.p13 chr2: 100,376,787-100,376,787 AFF3
    nsv5720663mobile element insertion2nstd211human GRCh38 chr2: 99,868,032-99,868,032 , GRCh37.p13 chr2: 100,484,494-100,484,494 AFF3
    nsv5717795mobile element insertion1nstd211human GRCh38 chr2: 99,768,173-99,768,173 , GRCh37.p13 chr2: 100,384,635-100,384,635 AFF3
    nsv5714690mobile element insertion1nstd211human GRCh38 chr2: 99,694,180-99,694,180 , GRCh37.p13 chr2: 100,310,642-100,310,642 AFF3, LOC105373504
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