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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5942510copy number variation1nstd209human GRCh38 chr16: 66,550,604-66,550,925 , GRCh37.p13 chr16: 66,584,507-66,584,828 TK2, CKLF, 1 more genes
    nsv5938195copy number variation1nstd209human GRCh38 chr16: 66,532,083-66,553,130 , GRCh37.p13 chr16: 66,565,986-66,587,033 TK2, CKLF, 1 more genes
    nsv5870130copy number variation1nstd209human GRCh38 chr16: 66,532,026-66,552,872 , GRCh37.p13 chr16: 66,565,929-66,586,775 TK2, CKLF, 1 more genes
    nsv5563255sequence alteration1nstd206human GRCh38 chr16: 66,545,588-66,550,793 , GRCh37.p13 chr16: 66,579,491-66,584,696 TK2, CKLF, 1 more genes
    nsv5358293translocation1nstd200human GRCh38 chr16: 66,537,553-66,537,553 , GRCh38 chr16: 66,537,473-66,537,473 , GRCh37.p13 chr16: 66,571,456-66,571,456 , GRCh37.p13 chr16: 66,571,376-66,571,376 TK2
    nsv5271437copy number variation1nstd204human GRCh38.p13 chr16: 66,514,201-66,529,200 , GRCh37.p13 chr16: 66,548,104-66,563,103 TK2
    nsv5155823mobile element insertion1nstd203human GRCh38 chr16: 66,513,106-66,513,115 , GRCh37.p13 chr16: 66,547,009-66,547,018 TK2
    nsv5140392mobile element insertion1nstd203human GRCh38 chr16: 66,547,833-66,547,849 , GRCh37.p13 chr16: 66,581,736-66,581,752 TK2
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv4993067copy number variation1nstd200human GRCh38 chr16: 66,542,138-66,543,079 , GRCh37.p13 chr16: 66,576,041-66,576,982 TK2
    nsv4993066copy number variation1nstd200human GRCh38 chr16: 66,526,399-66,526,460 , GRCh37.p13 chr16: 66,560,302-66,560,363 TK2
    nsv4993065copy number variation1nstd200human GRCh38 chr16: 66,522,922-66,522,990 , GRCh37.p13 chr16: 66,556,825-66,556,893 TK2
    nsv4993064copy number variation1nstd200human GRCh38 chr16: 66,520,387-66,521,434 , GRCh37.p13 chr16: 66,554,290-66,555,337 TK2
    nsv4993063copy number variation1nstd200human GRCh38 chr16: 66,505,933-66,510,096 , GRCh37.p13 chr16: 66,539,836-66,543,999 TK2
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4857447copy number variation1nstd200human GRCh37 chr16: 66,556,825-66,556,893 , GRCh38.p12 chr16: 66,522,922-66,522,990 TK2
    nsv4857446copy number variation1nstd200human GRCh37 chr16: 66,539,836-66,543,999 , GRCh38.p12 chr16: 66,505,933-66,510,096 TK2
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
    nsv4684382delins1nstd102humanPathogenic GRCh37 chr16: 66,578,756-66,584,584 , GRCh38 chr16: 66,544,853-66,550,681 TK2, CKLF, 1 more genes
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