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Items: 1 to 20 of 210

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5952007insertion1nstd209human GRCh38 chr8: 109,337,068-109,337,068 , GRCh37.p13 chr8: 110,349,297-110,349,297 ENY2
    nsv5908945copy number variation1nstd209human GRCh38 chr8: 109,338,347-109,338,519 , GRCh37.p13 chr8: 110,350,576-110,350,748 ENY2
    nsv5851996copy number variation1nstd209human GRCh38 chr8: 109,346,091-109,348,774 , GRCh37.p13 chr8: 110,358,320-110,361,003 ENY2
    nsv5696859mobile element insertion2nstd211human GRCh38 chr8: 109,337,081-109,337,081 , GRCh37.p13 chr8: 110,349,310-110,349,310 ENY2
    nsv5629283insertion1nstd207human GRCh38 chr8: 109,337,068-109,337,068 , GRCh37.p13 chr8: 110,349,297-110,349,297 ENY2
    nsv5252263copy number variation1nstd204human GRCh38.p13 chr8: 109,231,701-109,359,400 , GRCh37.p13 chr8: 110,243,930-110,371,629 NUDCD1, ENY2
    nsv5250759copy number variation1nstd204human GRCh38.p13 chr8: 109,320,117-109,343,840 , GRCh37.p13 chr8: 110,332,346-110,356,069 ENY2, NUDCD1
    nsv5246471copy number variation1nstd204human GRCh38.p13 chr8: 109,342,080-109,358,700 , GRCh37.p13 chr8: 110,354,309-110,370,929 ENY2
    nsv5118244mobile element insertion1nstd203human GRCh38 chr8: 109,337,072-109,337,081 , GRCh37.p13 chr8: 110,349,301-110,349,310 ENY2
    nsv5117221mobile element insertion1nstd203human GRCh38 chr8: 109,337,074-109,337,081 , GRCh37.p13 chr8: 110,349,303-110,349,310 ENY2
    nsv5114618mobile element insertion1nstd203human GRCh38 chr8: 109,337,067-109,337,081 , GRCh37.p13 chr8: 110,349,296-110,349,310 ENY2
    nsv5114441mobile element insertion1nstd203human GRCh38 chr8: 109,337,068-109,337,081 , GRCh37.p13 chr8: 110,349,297-110,349,310 ENY2
    nsv5113591mobile element insertion1nstd203human GRCh38 chr8: 109,337,066-109,337,081 , GRCh37.p13 chr8: 110,349,295-110,349,310 ENY2
    nsv5112889mobile element insertion1nstd203human GRCh38 chr8: 109,337,073-109,337,081 , GRCh37.p13 chr8: 110,349,302-110,349,310 ENY2
    nsv5111182mobile element insertion1nstd203human GRCh38 chr8: 109,337,081-109,337,081 , GRCh37.p13 chr8: 110,349,310-110,349,310 ENY2
    nsv5108462mobile element insertion1nstd203human GRCh38 chr8: 109,337,075-109,337,081 , GRCh37.p13 chr8: 110,349,304-110,349,310 ENY2
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4729617copy number variation1nstd102humanUncertain significance GRCh37 chr8: 109,694,757-110,374,218 , GRCh38.p12 chr8: 108,682,528-109,361,989 LOC101927413, TRHR, 6 more genes
    nsv4729071copy number variation1nstd102humanPathogenic GRCh37 chr8: 108,421,573-123,429,638 , GRCh38.p12 chr8: 107,409,345-122,417,399 RN7SL396P, LOC107986970, 124 more genes
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