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Items: 1 to 20 of 31

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3899037copy number variation1nstd102humanUncertain significance GRCh37 chr16: 52,464,934-52,676,323 , GRCh38.p12 chr16: 52,431,022-52,642,411 TOX3, LINC03064, 2 more genes
    nsv3912665copy number variation1nstd102humanPathogenic NCBI36 chr16: 45,842,056-52,712,889 , GRCh37 chr16: 47,284,555-54,155,388 , GRCh38 chr16: 47,250,644-54,121,476 TOX3, RPL10P14, 110 more genes
    nsv3918594copy number variation1nstd102humanPathogenic GRCh38 chr16: 50,784,329-55,566,715 , NCBI36 chr16: 49,375,741-54,158,128 , GRCh37 chr16: 50,818,240-55,600,627 TOX3, CASC22, 74 more genes
    nsv3917177copy number variation1nstd102humanPathogenic GRCh38 chr16: 49,570,553-53,467,065 , NCBI36 chr16: 48,161,965-52,058,478 , GRCh37 chr16: 49,604,464-53,500,977 TOX3, LOC107984901, 66 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 TOX3, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 TOX3, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 TOX3, LINC02175, 1877 more genes
    nsv3909417copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867 TOX3, PRSS53, 1868 more genes
    nsv3892266copy number variation2nstd102humanPathogenic GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654 TOX3, FTLP14, 1868 more genes
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 TOX3, LOC105371237, 985 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 TOX3, ATMIN, 826 more genes
    nsv3895555copy number variation1nstd102humanPathogenic GRCh37 chr16: 34,197,492-64,509,054 , GRCh38.p12 chr16: 34,963,121-64,475,151 TOX3, RSPRY1, 362 more genes
    nsv3918521copy number variation1nstd102humanPathogenic NCBI36 chr16: 48,276,933-66,993,116 , GRCh37 chr16: 49,719,432-68,435,615 , GRCh38 chr16: 49,685,521-68,401,712 TOX3, CYLD-AS2, 342 more genes
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 TOX3, LINC02140, 279 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 TOX3, CPNE2, 275 more genes
    nsv3912769copy number variation1nstd102humanBenign NCBI36 chr16: 31,862,658-88,822,254 , GRCh37.p13 chr16: 31,955,157-90,294,753 , GRCh38.p12 chr16: 31,943,836-90,228,345 TOX3, MAF, 985 more genes
    nsv3915341copy number variation1nstd102humanBenign NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 TOX3, GINS3, 985 more genes
    nsv3915118copy number variation1nstd102humanBenign NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 TOX3, ZFHX3, 985 more genes
    nsv3912663copy number variation1nstd102humanBenign NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 TOX3, SMG1P7, 985 more genes
    nsv3912156copy number variation1nstd102humanBenign NCBI36 chr16: 31,902,168-88,822,254 , GRCh37.p13 chr16: 31,994,667-90,294,753 , GRCh38.p12 chr16: 31,983,346-90,228,345 TOX3, IST1, 985 more genes
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