U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 134

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5930987copy number variation1nstd209human GRCh38 chr12: 56,470,194-56,470,916 , GRCh37.p13 chr12: 56,863,978-56,864,700 SPRYD4, GLS2
    nsv5927872copy number variation1nstd209human GRCh38 chr12: 56,476,193-56,476,632 , GRCh37.p13 chr12: 56,869,977-56,870,416 GLS2, SPRYD4
    nsv5510328copy number variation1nstd206human GRCh38 chr12: 56,472,874-56,472,938 , GRCh37.p13 chr12: 56,866,658-56,866,722 GLS2, SPRYD4
    nsv5503934copy number variation1nstd206human GRCh38 chr12: 56,470,195-56,470,917 , GRCh37.p13 chr12: 56,863,979-56,864,701 SPRYD4, GLS2
    nsv5355959translocation1nstd200human GRCh38 chr12: 56,470,195-56,470,195 , GRCh38 chr12: 56,470,917-56,470,917 , GRCh37.p13 chr12: 56,863,979-56,863,979 , GRCh37.p13 chr12: 56,864,701-56,864,701 GLS2, SPRYD4
    nsv5329782translocation1nstd200human GRCh37 chr12: 56,863,979-56,863,979 , GRCh37 chr12: 56,864,701-56,864,701 , GRCh38.p12 chr12: 56,470,917-56,470,917 , GRCh38.p12 chr12: 56,470,195-56,470,195 SPRYD4, GLS2
    nsv5310290copy number variation1nstd204human GRCh37.p13 chr12: 56,863,974-56,864,710 , GRCh38.p13 chr12: 56,470,190-56,470,926 GLS2, SPRYD4
    nsv5267790copy number variation1nstd204human GRCh37.p13 chr12: 56,781,185-56,989,684 , GRCh38.p13 chr12: 56,387,401-56,595,900 MIP, RBMS2, 7 more genes
    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
    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
    nsv4739946copy number variation1nstd199human GRCh37 chr12: 56,863,957-56,864,696 , GRCh38.p12 chr12: 56,470,173-56,470,912 SPRYD4, GLS2
    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
    nsv4670967copy number variation1nstd186human GRCh37 chr12: 56,863,978-56,864,701 , GRCh38.p12 chr12: 56,470,194-56,470,917 GLS2, SPRYD4
    nsv4615170copy number variation1nstd183human GRCh37 chr12: 56,863,978-56,864,701 , GRCh38.p12 chr12: 56,470,194-56,470,917 SPRYD4, GLS2
    nsv4430671copy number variation1nstd174human GRCh37 chr12: 56,863,978-56,864,799 , GRCh38.p12 chr12: 56,470,194-56,471,015 GLS2, SPRYD4
    nsv4390279copy number variation1nstd171human GRCh37 chr12: 56,863,979-56,864,701 , GRCh38.p12 chr12: 56,470,195-56,470,917 GLS2, SPRYD4
    nsv4345299sequence alteration1nstd166human GRCh37.p13 chr12: 56,858,903-56,864,124 , GRCh38.p12 chr12: 56,465,119-56,470,340 GLS2, SPRYD4
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center