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 120

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv7077264inversion1nstd229human GRCh38 chr9: 107,230,971-107,507,293 , GRCh37.p13 chr9: 109,993,252-110,269,574 RAD23B, LOC107987110, 6 more genes
    nsv7074978inversion1nstd229human GRCh38 chr9: 106,755,903-108,407,110 , GRCh37.p13 chr9: 109,518,184-111,169,390 LOC105376209, LINC01509, 31 more genes
    nsv6874739copy number variation1nstd229human GRCh38 chr9: 107,441,701-107,650,374 , GRCh37.p13 chr9: 110,203,982-110,412,655 RNU6-492P, KLF4, 5 more genes
    nsv6871477copy number variation1nstd229human GRCh38 chr9: 107,346,001-107,556,200 , GRCh37.p13 chr9: 110,108,282-110,318,481 KLF4, LOC107987111, 5 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6572915inversion1nstd223human GRCh38 chr9: 107,473,468-107,474,163 , GRCh37.p13 chr9: 110,235,749-110,236,444 RNU6-492P
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6290765copy number variation1nstd102humanUncertain significance GRCh37 chr9: 102,858,276-110,624,997 , GRCh38.p12 chr9: 100,095,994-107,862,716 RNF20, SMC2, 120 more genes
    nsv6137327copy number variation1nstd213human GRCh37 chr9: 109,340,000-112,470,001 , GRCh38.p12 chr9: 106,577,719-109,707,721 ACTL7A, TMEM245, 55 more genes
    nsv6136633copy number variation1nstd213human GRCh37 chr9: 110,220,000-110,410,001 , GRCh38.p12 chr9: 107,457,719-107,647,720 KLF4, HMGN2P32, 5 more genes
    nsv6136350copy number variation1nstd213human GRCh37 chr9: 109,820,000-110,360,001 , GRCh38.p12 chr9: 107,057,719-107,597,720 RAD23B, LOC340512, 11 more genes
    nsv5474485copy number variation1nstd206human GRCh38 chr9: 107,473,235-107,476,141 , GRCh37.p13 chr9: 110,235,516-110,238,422 RNU6-492P
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983052copy number variation1nstd200human GRCh38 chr9: 107,475,250-107,477,296 , GRCh37.p13 chr9: 110,237,531-110,239,577 RNU6-492P
    nsv4983051copy number variation1nstd200human GRCh38 chr9: 107,475,522-107,475,599 , GRCh37.p13 chr9: 110,237,803-110,237,880 RNU6-492P
    nsv4840107copy number variation1nstd200human GRCh37 chr9: 110,237,803-110,237,880 , GRCh38.p12 chr9: 107,475,522-107,475,599 RNU6-492P
    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