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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3910641copy number variation1nstd102humanLikely benign NCBI36 chr8: 9,438,832-9,462,254 , GRCh38 chr8: 9,543,912-9,567,334 , GRCh37 chr8: 9,401,422-9,424,844 TNKS
    nsv3896009copy number variation1nstd102humanBenign GRCh37 chr8: 9,479,127-9,500,876 , GRCh38.p12 chr8: 9,621,617-9,643,366 , GRCh38.p12 chr8|NW_018654717.1: 3,708,134-3,729,874 TNKS
    nsv3900974copy number variation1nstd102humanBenign GRCh37 chr8: 9,498,014-9,500,876 , GRCh38.p12 chr8: 9,640,504-9,643,366 , GRCh38.p12 chr8|NW_018654717.1: 3,708,134-3,710,996 TNKS
    nsv3896611copy number variation1nstd102humanBenign GRCh37 chr8: 9,471,265-9,500,692 , GRCh38.p12 chr8|NW_018654717.1: 3,708,318-3,737,737 , GRCh38.p12 chr8: 9,613,755-9,643,182 TNKS
    nsv3894503copy number variation1nstd102humanBenign GRCh37 chr8: 9,471,265-9,500,595 , GRCh38.p12 chr8: 9,613,755-9,643,085 , GRCh38.p12 chr8|NW_018654717.1: 3,708,415-3,737,737 TNKS
    nsv3899196copy number variation2nstd102humanBenign GRCh37 chr8: 9,479,127-9,500,692 , GRCh38.p12 chr8: 9,621,617-9,643,182 , GRCh38.p12 chr8|NW_018654717.1: 3,708,318-3,729,874 TNKS
    nsv3894515copy number variation1nstd102humanBenign GRCh37 chr8: 9,479,127-9,500,595 , GRCh38.p12 chr8|NW_018654717.1: 3,708,415-3,729,874 , GRCh38.p12 chr8: 9,621,617-9,643,085 TNKS
    nsv4674991copy number variation1nstd102humanUncertain significance GRCh37 chr8: 9,613,875-9,742,841 , GRCh38.p12 chr8: 9,756,365-9,885,331 , GRCh38.p12 chr8|NW_018654717.1: 3,463,581-3,595,206 TNKS
    nsv6291144copy number variation1nstd102humanUncertain significance GRCh37 chr8: 9,447,087-9,687,874 , GRCh38.p12 chr8|NW_018654717.1: 3,518,506-3,761,904 , GRCh38.p12 chr8: 9,589,577-9,830,364 TNKS, MIR597
    nsv4729091copy number variation1nstd102humanUncertain significance GRCh37 chr8: 9,511,554-9,647,023 , GRCh38.p12 chr8: 9,654,044-9,789,513 , GRCh38.p12 chr8|NW_018654717.1: 3,559,554-3,697,464 TNKS, MIR597
    nsv3902768copy number variation1nstd102humanUncertain significance GRCh37 chr8: 9,556,061-9,852,711 , GRCh38.p12 chr8: 9,698,551-9,995,201 , GRCh38.p12 chr8|NW_018654717.1: 3,353,194-3,653,001 TNKS, MIR124-1HG, 3 more genes
    nsv3904746copy number variation1nstd102humanUncertain significance GRCh37 chr8: 9,551,476-9,803,102 , GRCh38.p12 chr8|NW_018654717.1: 3,403,130-3,657,587 , GRCh38.p12 chr8: 9,693,966-9,945,592 TNKS, MIR124-1HG, 2 more genes
    nsv4676036copy number variation1nstd102humanUncertain significance GRCh37 chr8: 9,635,218-9,819,173 , GRCh38.p12 chr8|NW_018654717.1: 3,386,725-3,571,355 , GRCh38.p12 chr8: 9,777,708-9,961,663 TNKS, MIR124-1, 1 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 TNKS, LOC101928016, 568 more genes
    nsv3917350copy number variation2nstd102humanPathogenic GRCh37 chr8: 2,292,235-27,361,796 , GRCh38 chr8: 2,475,295-27,504,279 , NCBI36 chr8: 2,121,457-27,417,713 TNKS, LINC03022, 472 more genes
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 TNKS, ENTPD4, 447 more genes
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 TNKS, ZNF705B, 357 more genes
    nsv4455719copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-14,214,722 , GRCh38.p12 chr8: 208,048-14,357,213 TNKS, MIR598, 312 more genes
    nsv4685988copy number variation1nstd102humanPathogenic GRCh37 chr8: 161,516-11,516,619 , GRCh38.p12 chr8: 211,516-11,659,110 TNKS, ZNF705B, 232 more genes
    nsv7148131copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,501-11,142,629 , GRCh38.p12 chr8: 60,501-11,285,120 TNKS, XKR6, 224 more genes
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