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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970274insertion1nstd209human GRCh38 chr16: 87,981,951-87,981,951 , GRCh37.p13 chr16: 88,015,557-88,015,557 BANP
    nsv5946334copy number variation1nstd209human GRCh38 chr16: 88,010,757-88,010,887 , GRCh37.p13 chr16: 88,044,363-88,044,493 BANP
    nsv5945742copy number variation1nstd209human GRCh38 chr16: 87,997,510-87,997,715 , GRCh37.p13 chr16: 88,031,116-88,031,321 BANP
    nsv5943518copy number variation1nstd209human GRCh38 chr16: 88,053,092-88,053,835 , GRCh37.p13 chr16: 88,086,698-88,087,441 BANP
    nsv5940404copy number variation1nstd209human GRCh38 chr16: 88,053,484-88,053,741 , GRCh37.p13 chr16: 88,087,090-88,087,347 BANP
    nsv5938870copy number variation1nstd209human GRCh38 chr16: 87,944,683-87,949,988 , GRCh37.p13 chr16: 87,978,289-87,983,594 LOC107984816, BANP
    nsv5937806copy number variation1nstd209human GRCh38 chr16: 87,998,562-87,998,611 , GRCh37.p13 chr16: 88,032,168-88,032,217 BANP
    nsv5935413copy number variation1nstd209human GRCh38 chr16: 88,001,256-88,001,313 , GRCh37.p13 chr16: 88,034,862-88,034,919 BANP
    nsv5933861copy number variation1nstd209human GRCh38 chr16: 87,987,685-87,987,737 , GRCh37.p13 chr16: 88,021,291-88,021,343 BANP
    nsv5931534copy number variation1nstd209human GRCh38 chr16: 88,009,841-88,010,023 , GRCh37.p13 chr16: 88,043,447-88,043,629 BANP
    nsv5929882copy number variation1nstd209human GRCh38 chr16: 87,948,193-87,948,246 , GRCh37.p13 chr16: 87,981,799-87,981,852 BANP
    nsv5929727copy number variation1nstd209human GRCh38 chr16: 88,029,539-88,032,796 , GRCh37.p13 chr16: 88,063,145-88,066,402 BANP
    nsv5929613copy number variation1nstd209human GRCh38 chr16: 88,053,415-88,053,948 , GRCh37.p13 chr16: 88,087,021-88,087,554 BANP
    nsv5928975copy number variation1nstd209human GRCh38 chr16: 88,062,986-88,126,515 , GRCh37.p13 chr16: 88,096,592-88,160,121 BANP, LOC400553
    nsv5883257copy number variation1nstd209human GRCh38 chr16: 87,944,729-87,950,040 , GRCh37.p13 chr16: 87,978,335-87,983,646 BANP, LOC107984816
    nsv5876978copy number variation1nstd209human GRCh38 chr16: 88,063,017-88,077,855 , GRCh37.p13 chr16: 88,096,623-88,111,461 BANP
    nsv5870648copy number variation1nstd209human GRCh38 chr16: 88,029,435-88,032,787 , GRCh37.p13 chr16: 88,063,041-88,066,393 BANP
    nsv5711628mobile element insertion2nstd211human GRCh38 chr16: 88,045,147-88,045,147 , GRCh37.p13 chr16: 88,078,753-88,078,753 BANP
    nsv5673006copy number variation1nstd102humanPathogenic GRCh37 chr16: 87,636,753-88,505,740 , GRCh38.p12 chr16: 87,603,147-88,439,332 LOC107984816, BANP, 15 more genes
    nsv5664285insertion1nstd207human GRCh38 chr16: 88,054,119-88,054,119 , GRCh37.p13 chr16: 88,087,725-88,087,725 BANP
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