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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5500933copy number variation1nstd206human GRCh38 chr12: 56,992,138-56,993,911 , GRCh37.p13 chr12: 57,385,922-57,387,695 GPR182
    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
    nsv4985654copy number variation1nstd200human GRCh38 chr12: 56,991,391-56,991,632 , GRCh37.p13 chr12: 57,385,175-57,385,416 GPR182
    nsv4972909copy number variation1nstd200human GRCh38 chr12: 56,992,216-56,993,838 , GRCh37.p13 chr12: 57,386,000-57,387,622 GPR182
    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
    nsv4675143copy number variation1nstd102humanPathogenic GRCh37 chr12: 55,552,371-62,126,304 , GRCh38.p12 chr12: 55,158,587-61,732,523 OR6C71P, METTL1, 183 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 , OR5BT1P, 2441 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 , RNA5SP369, 2454 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 , RNU4ATAC16P, 2452 more genes
    nsv3169098inversion1nstd158human GRCh37 chr12: 28,095,967-121,612,723 , GRCh38.p12 chr12: 27,943,034-121,174,920 , ACACB, 1642 more genes
    nsv3169084inversion1nstd158human GRCh37 chr12: 25,261,327-66,452,514 , GRCh38.p12 chr12: 25,108,393-66,058,734 , ASIC1, 835 more genes
    nsv3168746inversion1nstd158human GRCh37 chr12: 2,444,756-66,452,522 , GRCh38.p12 chr12: 2,335,590-66,058,742 , A2M, 1361 more genes
    nsv3167759inversion1nstd158human GRCh37 chr12: 24,267,124-66,452,483 , GRCh38.p12 chr12: 24,114,190-66,058,703 , ASIC1, 851 more genes
    nsv2740531copy number variation1nstd130human NCBI36 chr12: 49,559,698-128,874,436 , GRCh37.p13 chr12: 51,273,431-130,308,483 , GRCh38.p12 chr12: 50,879,648-129,823,938 , LINC01234, 1477 more genes
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