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 757

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146653copy number variation1nstd232human GRCh37.p13 chr12: 718,386-718,449 , GRCh38.p12 chr12: 609,220-609,283 NINJ2
    nsv7144420copy number variation1nstd232human GRCh37.p13 chr12: 691,440-691,559 , GRCh38.p12 chr12: 582,274-582,393 NINJ2
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7077356inversion1nstd229human GRCh38 chr12: 559,617-722,794 , GRCh37.p13 chr12: 668,783-831,960 NINJ2, LOC105369595, 5 more genes
    nsv7076516inversion1nstd229human GRCh38 chr12: 546,745-697,602 , GRCh37.p13 chr12: 655,911-806,768 NINJ2, LINC02455, 5 more genes
    nsv7068928inversion1nstd229human GRCh38 chr12: 583,436-614,455 , GRCh37.p13 chr12: 692,602-723,621 LOC105369595, RNU7-103P, 1 more genes
    nsv7067247inversion1nstd229human GRCh38 chr12: 577,362-800,666 , GRCh37.p13 chr12: 686,528-909,832 NINJ2, LOC101929432, 6 more genes
    nsv7063814inversion1nstd229human GRCh38 chr12: 525,152-790,509 , GRCh37.p13 chr12: 634,318-899,675 NINJ2, LINC02455, 7 more genes
    nsv7059434inversion1nstd229human GRCh38 chr12: 372,635-565,245 , GRCh37.p13 chr12: 481,801-674,411 CCDC77, B4GALNT3, 3 more genes
    nsv6917926copy number variation1nstd229human GRCh38 chr12: 323,157-645,016 , GRCh37.p13 chr12: 432,323-754,182 B4GALNT3, NINJ2, 6 more genes
    nsv6917607copy number variation1nstd229human GRCh38 chr12: 191,283-1,336,922 , GRCh37.p13 chr12: 300,449-1,446,088 RNU7-103P, NINJ2, 18 more genes
    nsv6916580copy number variation1nstd229human GRCh38 chr12: 385,701-565,300 , GRCh37.p13 chr12: 494,867-674,466 B4GALNT3, CCDC77, 3 more genes
    nsv6915312copy number variation1nstd229human GRCh38 chr12: 645,249-672,858 , GRCh37.p13 chr12: 754,415-782,024 NINJ2, NINJ2-AS1
    nsv6911693copy number variation1nstd229human GRCh38 chr12: 471,012-635,095 , GRCh37.p13 chr12: 580,178-744,261 NINJ2, RNU7-103P, 3 more genes
    nsv6910656copy number variation1nstd229human GRCh38 chr12: 620,314-623,930 , GRCh37.p13 chr12: 729,480-733,096 NINJ2
    nsv6908516copy number variation1nstd229human GRCh38 chr12: 574,365-574,495 , GRCh37.p13 chr12: 683,531-683,661 NINJ2
    nsv6908172copy number variation1nstd229human GRCh38 chr12: 599,763-619,260 , GRCh37.p13 chr12: 708,929-728,426 NINJ2
    nsv6906808copy number variation1nstd229human GRCh38 chr12: 655,757-661,183 , GRCh37.p13 chr12: 764,923-770,349 NINJ2
    nsv6906102copy number variation1nstd229human GRCh38 chr12: 602,201-605,200 , GRCh37.p13 chr12: 711,367-714,366 NINJ2
    nsv6905386copy number variation1nstd229human GRCh38 chr12: 573,726-578,296 , GRCh37.p13 chr12: 682,892-687,462 NINJ2
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

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