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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965250insertion1nstd209human GRCh38 chr2: 218,711,870-218,711,870 , GRCh37.p13 chr2: 219,576,593-219,576,593 TTLL4
    nsv5900821copy number variation1nstd209human GRCh38 chr2: 218,710,874-218,710,927 , GRCh37.p13 chr2: 219,575,597-219,575,650 TTLL4
    nsv5689668mobile element insertion2nstd211human GRCh38 chr2: 218,711,886-218,711,886 , GRCh37.p13 chr2: 219,576,609-219,576,609 TTLL4
    nsv5622244insertion1nstd207human GRCh38 chr2: 218,711,870-218,711,870 , GRCh37.p13 chr2: 219,576,593-219,576,593 TTLL4
    nsv5613452insertion1nstd207human GRCh38 chr2: 218,741,217-218,741,217 , GRCh37.p13 chr2: 219,605,940-219,605,940 TTLL4
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5452651copy number variation1nstd206human GRCh38 chr2: 218,756,884-218,789,439 , GRCh37.p13 chr2: 219,621,607-219,654,162 CYP27A1, TTLL4
    nsv5435077copy number variation1nstd206human GRCh38 chr2: 218,720,628-218,720,761 , GRCh37.p13 chr2: 219,585,351-219,585,484 TTLL4
    nsv5405397mobile element insertion1nstd206human GRCh38 chr2: 218,711,870-218,711,870 , GRCh37.p13 chr2: 219,576,593-219,576,593 TTLL4
    nsv5377356translocation1nstd200human GRCh38 chr3: 128,953,543-128,953,543 , GRCh38 chr2: 218,726,104-218,726,104 , GRCh37.p13 chr2: 219,590,827-219,590,827 , GRCh37.p13 chr3: 128,672,386-128,672,386 CFAP92, TTLL4
    nsv5361324translocation1nstd200human GRCh38 chr2: 218,754,446-218,754,446 , GRCh38 chr2: 218,754,504-218,754,504 , GRCh37.p13 chr2: 219,619,169-219,619,169 , GRCh37.p13 chr2: 219,619,227-219,619,227 TTLL4
    nsv5361323translocation1nstd200human GRCh38 chr2: 218,719,564-218,719,564 , GRCh38 chr2: 218,719,649-218,719,649 , GRCh37.p13 chr2: 219,584,287-219,584,287 , GRCh37.p13 chr2: 219,584,372-219,584,372 TTLL4
    nsv5342204translocation1nstd200human GRCh37 chr3: 128,672,386-128,672,386 , GRCh37 chr2: 219,590,827-219,590,827 , GRCh38.p12 chr2: 218,726,104-218,726,104 , GRCh38.p12 chr3: 128,953,543-128,953,543 TTLL4, CFAP92
    nsv5079487mobile element insertion1nstd203human GRCh38 chr2: 218,711,874-218,711,886 , GRCh37.p13 chr2: 219,576,597-219,576,609 TTLL4
    nsv5077782mobile element insertion1nstd203human GRCh38 chr2: 218,711,877-218,711,886 , GRCh37.p13 chr2: 219,576,600-219,576,609 TTLL4
    nsv5077355mobile element insertion1nstd203human GRCh38 chr2: 218,711,865-218,711,870 , GRCh37.p13 chr2: 219,576,588-219,576,593 TTLL4
    nsv5075797mobile element insertion1nstd203human GRCh38 chr2: 218,711,884-218,711,884 , GRCh37.p13 chr2: 219,576,607-219,576,607 TTLL4
    nsv5075481mobile element insertion1nstd203human GRCh38 chr2: 218,711,886-218,711,886 , GRCh37.p13 chr2: 219,576,609-219,576,609 TTLL4
    nsv5074486mobile element insertion1nstd203human GRCh38 chr2: 218,711,871-218,711,886 , GRCh37.p13 chr2: 219,576,594-219,576,609 TTLL4
    nsv5073174mobile element insertion1nstd203human GRCh38 chr2: 218,711,882-218,711,882 , GRCh37.p13 chr2: 219,576,605-219,576,605 TTLL4
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