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Items: 1 to 20 of 488

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5954616insertion1nstd209human GRCh38 chr1: 45,735,955-45,735,955 , GRCh37.p13 chr1: 46,201,627-46,201,627 IPP
    nsv5868917copy number variation1nstd209human GRCh38 chr1: 45,741,614-45,741,925 , GRCh37.p13 chr1: 46,207,286-46,207,597 IPP
    nsv5830210copy number variation1nstd209human GRCh38 chr1: 45,699,063-45,703,128 , GRCh37.p13 chr1: 46,164,735-46,168,800 IPP
    nsv5830209copy number variation1nstd209human GRCh38 chr1: 45,680,212-45,697,612 , GRCh37.p13 chr1: 46,145,884-46,163,284 TMEM69, GPBP1L1, 1 more genes
    nsv5830029copy number variation1nstd209human GRCh38 chr1: 45,710,337-45,712,665 , GRCh37.p13 chr1: 46,176,009-46,178,337 IPP
    nsv5829734copy number variation1nstd209human GRCh38 chr1: 45,739,392-45,762,911 , GRCh37.p13 chr1: 46,205,064-46,228,583 IPP, LOC105378693
    nsv5829733copy number variation1nstd209human GRCh38 chr1: 45,729,135-45,733,334 , GRCh37.p13 chr1: 46,194,807-46,199,006 IPP
    nsv5829732copy number variation1nstd209human GRCh38 chr1: 45,714,216-45,721,713 , GRCh37.p13 chr1: 46,179,888-46,187,385 IPP
    nsv5829731copy number variation1nstd209human GRCh38 chr1: 45,713,066-45,715,415 , GRCh37.p13 chr1: 46,178,738-46,181,087 IPP
    nsv5829730copy number variation1nstd209human GRCh38 chr1: 45,699,663-45,708,580 , GRCh37.p13 chr1: 46,165,335-46,174,252 IPP
    nsv5729256mobile element insertion1nstd211human GRCh38 chr1: 45,730,243-45,730,243 , GRCh37.p13 chr1: 46,195,915-46,195,915 IPP
    nsv5688752mobile element insertion1nstd211human GRCh38 chr1: 45,718,148-45,718,148 , GRCh37.p13 chr1: 46,183,820-46,183,820 IPP
    nsv5677004mobile element insertion2nstd211human GRCh38 chr1: 45,694,124-45,694,124 , GRCh37.p13 chr1: 46,159,796-46,159,796 IPP, TMEM69
    nsv5621859insertion1nstd207human GRCh38 chr1: 45,703,341-45,703,341 , GRCh37.p13 chr1: 46,169,013-46,169,013 IPP
    nsv5609996insertion1nstd207human GRCh38 chr1: 45,710,951-45,710,951 , GRCh37.p13 chr1: 46,176,623-46,176,623 IPP
    nsv5604570insertion1nstd207human GRCh38 chr1: 45,709,107-45,709,107 , GRCh37.p13 chr1: 46,174,779-46,174,779 IPP
    nsv5576285copy number variation1nstd207human GRCh38 chr1: 45,709,596-45,709,993 , GRCh37.p13 chr1: 46,175,268-46,175,665 IPP
    nsv5572824copy number variation1nstd207human GRCh38 chr1: 45,724,893-45,725,342 , GRCh37.p13 chr1: 46,190,565-46,191,014 IPP
    nsv5565880copy number variation1nstd207human GRCh38 chr1: 45,741,614-45,741,925 , GRCh37.p13 chr1: 46,207,286-46,207,597 IPP
    nsv5563104sequence alteration1nstd206human GRCh38 chr1: 45,733,110-46,239,402 , GRCh37.p13 chr1: 46,198,782-46,705,074 IPP, LOC101929626, 11 more genes
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