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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885762copy number variation1nstd209human GRCh38 chr1: 186,348,461-186,348,510 , GRCh37.p13 chr1: 186,317,593-186,317,642 TPR
    nsv5876769copy number variation1nstd209human GRCh38 chr1: 186,327,069-186,327,278 , GRCh37.p13 chr1: 186,296,201-186,296,410 TPR
    nsv5872712copy number variation1nstd209human GRCh38 chr1: 186,327,162-186,327,265 , GRCh37.p13 chr1: 186,296,294-186,296,397 TPR
    nsv5682651mobile element insertion2nstd211human GRCh38 chr1: 186,370,596-186,370,596 , GRCh37.p13 chr1: 186,339,728-186,339,728 TPR
    nsv5617630insertion1nstd207human GRCh38 chr1: 186,327,266-186,327,266 , GRCh37.p13 chr1: 186,296,398-186,296,398 TPR
    nsv5605910insertion1nstd207human GRCh38 chr1: 186,327,281-186,327,281 , GRCh37.p13 chr1: 186,296,413-186,296,413 TPR
    nsv5582560copy number variation1nstd207human GRCh38 chr1: 186,327,071-186,327,173 , GRCh37.p13 chr1: 186,296,203-186,296,305 TPR
    nsv5437587copy number variation1nstd206human GRCh38 chr1: 186,317,408-186,317,491 , GRCh37.p13 chr1: 186,286,540-186,286,623 TPR
    nsv5403140mobile element insertion1nstd206human GRCh38 chr1: 186,370,596-186,370,647 , GRCh37.p13 chr1: 186,339,728-186,339,779 TPR
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5075458mobile element insertion1nstd203human GRCh38 chr1: 186,370,579-186,370,596 , GRCh37.p13 chr1: 186,339,711-186,339,728 TPR
    nsv4904109copy number variation1nstd200human GRCh38 chr1: 186,353,247-186,602,096 , GRCh37.p13 chr1: 186,322,379-186,571,228 TPR, PDC-AS1, 3 more genes
    nsv4781319copy number variation1nstd200human GRCh37 chr1: 186,322,374-186,571,242 , GRCh38.p12 chr1: 186,353,242-186,602,110 LOC100131939, TPR, 3 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4736335copy number variation1nstd199human GRCh37 chr1: 186,296,145-186,296,218 , GRCh38.p12 chr1: 186,327,013-186,327,086 TPR
    nsv4673925copy number variation1nstd102humanPathogenic GRCh37 chr1: 177,551,193-199,599,056 , GRCh38.p12 chr1: 177,582,058-199,629,928 QSOX1, PTPRC, 263 more genes
    nsv4580190copy number variation1nstd183human GRCh37 chr1: 186,307,206-186,308,594 , GRCh38.p12 chr1: 186,338,074-186,339,462 TPR
    nsv4580189copy number variation1nstd183human GRCh37 chr1: 186,282,656-186,283,586 , GRCh38.p12 chr1: 186,313,524-186,314,454 TPR, PRG4
    nsv4579938copy number variation1nstd183human GRCh37 chr1: 186,324,657-186,325,422 , GRCh38.p12 chr1: 186,355,525-186,356,290 TPR
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