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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045032inversion1nstd229human GRCh38 chr6: 49,872,474-49,959,976 , GRCh37.p13 chr6: 49,840,187-49,927,689 DEFB133, CRISP1, 1 more genes
    nsv6795271copy number variation1nstd229human GRCh38 chr6: 49,332,174-50,024,818 , GRCh37.p13 chr6: 49,299,844-49,992,531 DEFB114, LOC101927020, 16 more genes
    nsv6791174copy number variation1nstd229human GRCh38 chr6: 49,494,055-50,046,260 , GRCh37.p13 chr6: 49,461,768-50,013,973 DEFB110, CRISP1, 13 more genes
    nsv6788988copy number variation1nstd229human GRCh38 chr6: 49,959,907-50,381,479 , GRCh37.p13 chr6: 49,927,620-50,349,192 LOC100505985, DEFB112, 3 more genes
    nsv6400045copy number variation1nstd223human GRCh38 chr6: 49,960,701-49,961,300 , GRCh37.p13 chr6: 49,928,414-49,929,013 DEFB114
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 ACTG1P9, CRISP1, 245 more genes
    nsv6290935copy number variation1nstd102humanUncertain significance GRCh37 chr6: 49,459,881-50,012,992 , GRCh38.p12 chr6: 49,492,168-50,045,279 DEFB133, PGK2, 14 more genes
    nsv6136508copy number variation1nstd213human GRCh37 chr6: 49,700,000-50,020,001 , GRCh38.p12 chr6: 49,732,287-50,052,288 DEFB113, LOC101927020, 8 more genes
    nsv6135921copy number variation1nstd213human GRCh37 chr6: 34,700,000-52,650,001 , GRCh38.p12 chr6: 34,732,223-52,785,203 ACTG1P9, CRISP1, 361 more genes
    nsv5845532copy number variation1nstd209human GRCh38 chr6: 49,962,366-49,967,909 , GRCh37.p13 chr6: 49,930,079-49,935,622 DEFB113, DEFB114
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5473510copy number variation1nstd206human GRCh38 chr6: 49,961,984-49,962,111 , GRCh37.p13 chr6: 49,929,697-49,929,824 DEFB114
    nsv5362957translocation1nstd200human GRCh38 chr6: 49,962,111-49,962,111 , GRCh38 chr6: 49,961,984-49,961,984 , GRCh37.p13 chr6: 49,929,824-49,929,824 , GRCh37.p13 chr6: 49,929,697-49,929,697 DEFB114
    nsv5221557copy number variation1nstd204human GRCh38.p13 chr6: 49,961,101-49,967,900 , GRCh37.p13 chr6: 49,928,814-49,935,613 DEFB114, DEFB113
    nsv5104772mobile element insertion1nstd203human GRCh38 chr6: 49,962,286-49,962,305 , GRCh37.p13 chr6: 49,929,999-49,930,018 DEFB114
    nsv4941362copy number variation1nstd200human GRCh38 chr6: 49,962,981-49,971,925 , GRCh37.p13 chr6: 49,930,694-49,939,638 DEFB113, DEFB114
    nsv4816356copy number variation1nstd200human GRCh37 chr6: 49,929,697-49,929,824 , GRCh38.p12 chr6: 49,961,984-49,962,111 DEFB114
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
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