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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3888273copy number variation1nstd102humanPathogenic GRCh38 chr17: 46,031,456-46,082,562 , GRCh37 chr17: 44,108,822-44,159,928 KANSL1
    nsv4769345copy number variation1nstd102humanPathogenic GRCh38 chr17: 46,050,658-46,055,365 , GRCh37 chr17: 44,128,024-44,132,731 KANSL1
    nsv3907452copy number variation1nstd102humanBenign GRCh37 chr17: 44,108,100-44,129,253 , GRCh38.p12 chr17|NT_187663.1: 732,846-753,997 , GRCh38.p12 chr17: 46,030,734-46,051,887 KANSL1
    nsv3896024copy number variation1nstd102humanBenign GRCh37 chr17: 44,165,803-44,212,727 , GRCh38.p12 chr17|NT_187663.1: 790,538-837,468 , GRCh38.p12 chr17: 46,088,437-46,135,361 KANSL1
    nsv3895519copy number variation1nstd102humanBenign GRCh37 chr17: 44,165,803-44,197,806 , GRCh38.p12 chr17: 46,088,437-46,120,440 , GRCh38.p12 chr17|NT_187663.1: 790,538-822,537 KANSL1
    nsv3894707copy number variation1nstd102humanBenign GRCh37 chr17: 44,164,918-44,194,646 , GRCh38.p12 chr17|NT_187663.1: 789,653-819,378 , GRCh38.p12 chr17: 46,087,552-46,117,280 KANSL1
    nsv3891937copy number variation1nstd102humanBenign GRCh37 chr17: 44,274,985-44,292,319 , GRCh38.p12 chr17: 46,197,619-46,214,953 , GRCh38.p12 chr17|NT_187663.1: 899,723-917,126 KANSL1
    nsv3907272copy number variation1nstd102humanBenign GRCh37 chr17: 44,166,455-44,179,155 , GRCh38.p12 chr17|NT_187663.1: 791,190-803,894 , GRCh38.p12 chr17: 46,089,089-46,101,789 KANSL1
    nsv3907315copy number variation1nstd102humanBenign GRCh37 chr17: 44,213,187-44,223,107 , GRCh38.p12 chr17: 46,135,821-46,145,741 , GRCh38.p12 chr17|NT_187663.1: 837,927-847,847 KANSL1
    nsv3905612copy number variation1nstd102humanBenign GRCh37 chr17: 44,249,838-44,259,539 , GRCh38.p12 chr17: 46,172,472-46,182,173 , GRCh38.p12 chr17|NT_187663.1: 874,577-884,275 KANSL1
    nsv3903217copy number variation1nstd102humanBenign GRCh37 chr17: 44,285,531-44,293,981 , GRCh38.p12 chr17: 46,208,165-46,216,615 , GRCh38.p12 chr17|NT_187663.1: 910,267-918,788 KANSL1
    nsv3898617copy number variation1nstd102humanBenign GRCh37 chr17: 44,285,683-44,293,981 , GRCh38.p12 chr17|NT_187663.1: 910,419-918,788 , GRCh38.p12 chr17: 46,208,317-46,216,615 KANSL1
    nsv3894201copy number variation1nstd102humanBenign GRCh37 chr17: 44,285,531-44,292,319 , GRCh38.p12 chr17: 46,208,165-46,214,953 , GRCh38.p12 chr17|NT_187663.1: 910,267-917,126 KANSL1
    nsv3899335copy number variation1nstd102humanBenign GRCh37 chr17: 44,275,035-44,277,825 , GRCh38.p12 chr17: 46,197,669-46,200,459 , GRCh38.p12 chr17|NT_187663.1: 899,773-902,561 KANSL1
    nsv7094898copy number variation1nstd102humanUncertain significance GRCh37 chr17: 44,108,822-44,159,928 , GRCh38.p12 chr17: 46,031,456-46,082,562 , GRCh38.p12 chr17|NT_187663.1: 733,568-784,663 KANSL1
    nsv4683033copy number variation1nstd102humanUncertain significance GRCh37 chr17: 44,108,822-44,145,053 , GRCh38.p12 chr17|NT_187663.1: 733,568-769,786 , GRCh38.p12 chr17: 46,031,456-46,067,687 KANSL1
    nsv3874053copy number variation1nstd102humanUncertain significance GRCh38 chr17: 46,031,456-46,050,724 , GRCh37 chr17: 44,108,822-44,128,090 KANSL1
    nsv6310224copy number variation1nstd102humanUncertain significance GRCh37 chr17: 44,159,787-44,159,928 , GRCh38.p12 chr17|NT_187663.1: 784,522-784,663 , GRCh38.p12 chr17: 46,082,421-46,082,562 KANSL1
    nsv3895931copy number variation1nstd102humanBenign GRCh37 chr17: 44,165,803-44,266,531 , GRCh38.p12 chr17: 46,088,437-46,189,165 , GRCh38.p12 chr17|NT_187663.1: 790,538-891,269 KANSL1, LOC107985027
    nsv3899440copy number variation1nstd102humanBenign GRCh37 chr17: 44,164,918-44,259,919 , GRCh38.p12 chr17: 46,087,552-46,182,553 , GRCh38.p12 chr17|NT_187663.1: 789,653-884,655 KANSL1, LOC107985027
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