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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961406insertion1nstd209human GRCh38 chr2: 171,558,477-171,558,477 , GRCh37.p13 chr2: 172,414,987-172,414,987 CYBRD1
    nsv5889431copy number variation1nstd209human GRCh38 chr2: 171,558,414-171,558,476 , GRCh37.p13 chr2: 172,414,924-172,414,986 CYBRD1
    nsv5685748mobile element insertion2nstd211human GRCh38 chr2: 171,545,967-171,545,967 , GRCh37.p13 chr2: 172,402,477-172,402,477 CYBRD1
    nsv5622902insertion1nstd207human GRCh38 chr2: 171,535,514-171,535,514 , GRCh37.p13 chr2: 172,392,024-172,392,024 CYBRD1
    nsv5618637insertion1nstd207human GRCh38 chr2: 171,558,477-171,558,477 , GRCh37.p13 chr2: 172,414,987-172,414,987 CYBRD1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5442379copy number variation1nstd206human GRCh38 chr2: 171,528,396-171,528,472 , GRCh37.p13 chr2: 172,384,906-172,384,982 CYBRD1
    nsv5437928copy number variation1nstd206human GRCh38 chr2: 171,541,925-171,542,080 , GRCh37.p13 chr2: 172,398,435-172,398,590 CYBRD1
    nsv5407634mobile element insertion1nstd206human GRCh38 chr2: 171,545,967-171,546,018 , GRCh37.p13 chr2: 172,402,477-172,402,528 CYBRD1
    nsv5381341copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,999,572-182,774,361 , GRCh38.p12 chr2: 171,143,062-181,909,634 ALDH7A1P2, LOC101927055, 174 more genes
    nsv5381164copy number variation1nstd102humanUncertain significance GRCh37 chr2: 172,291,068-172,750,744 , GRCh38.p12 chr2: 171,434,558-171,894,234 SLC25A12, METTL8, 7 more genes
    nsv5175106mobile element insertion1nstd203human GRCh38 chr2: 171,525,606-171,525,622 , GRCh37.p13 chr2: 172,382,116-172,382,132 CYBRD1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4926496copy number variation1nstd200human GRCh38 chr2: 171,548,456-171,549,571 , GRCh37.p13 chr2: 172,404,966-172,406,081 CYBRD1
    nsv4926495copy number variation1nstd200human GRCh38 chr2: 171,541,925-171,542,080 , GRCh37.p13 chr2: 172,398,435-172,398,590 CYBRD1
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 RBM45, LOC102724194, 258 more genes
    nsv4756836insertion1nstd199human GRCh37 chr2: 172,392,023-172,392,023 , GRCh38.p12 chr2: 171,535,513-171,535,513 CYBRD1
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