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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5935557copy number variation1nstd209human GRCh38 chr12: 69,261,500-69,261,568 , GRCh37.p13 chr12: 69,655,280-69,655,348 CPSF6
    nsv5863341copy number variation1nstd209human GRCh38 chr12: 69,271,596-69,272,923 , GRCh37.p13 chr12: 69,665,376-69,666,703 MIR1279, CPSF6
    nsv5663806insertion1nstd207human GRCh38 chr12: 69,261,500-69,261,500 , GRCh37.p13 chr12: 69,655,280-69,655,280 CPSF6
    nsv5556951sequence alteration1nstd206human GRCh38 chr12: 68,612,001-69,442,414 , GRCh37.p13 chr12: 69,005,781-69,836,194 , LYZ, 22 more genes
    nsv5508803copy number variation1nstd206human GRCh38 chr12: 69,261,500-69,261,569 , GRCh37.p13 chr12: 69,655,280-69,655,349 CPSF6
    nsv5495340copy number variation1nstd206human GRCh38 chr12: 69,248,463-69,248,952 , GRCh37.p13 chr12: 69,642,243-69,642,732 CPSF6
    nsv5433583mobile element insertion1nstd206human GRCh38 chr12: 69,248,290-69,248,341 , GRCh37.p13 chr12: 69,642,070-69,642,121 CPSF6
    nsv5365101translocation1nstd200human GRCh38 chr12: 69,238,924-69,238,924 , GRCh38 chr12: 69,231,773-69,231,773 , GRCh37.p13 chr12: 69,625,553-69,625,553 , GRCh37.p13 chr12: 69,632,704-69,632,704 CPSF6
    nsv5133519mobile element insertion1nstd203human GRCh38 chr12: 69,248,281-69,248,290 , GRCh37.p13 chr12: 69,642,061-69,642,070 CPSF6
    nsv5121645mobile element insertion1nstd203human GRCh38 chr12: 69,254,227-69,254,241 , GRCh37.p13 chr12: 69,648,007-69,648,021 CPSF6
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv4995127copy number variation1nstd200human GRCh38 chr12: 69,250,217-69,250,488 , GRCh37.p13 chr12: 69,643,997-69,644,268 CPSF6
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4729265copy number variation1nstd102humanPathogenic GRCh37 chr12: 68,572,386-70,833,868 , GRCh38.p12 chr12: 68,178,606-70,440,088 LINC02384, LOC101928002, 47 more genes
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