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 449

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5909062copy number variation1nstd209human GRCh38 chr9: 137,079,827-137,079,930 , GRCh37.p13 chr9: 139,974,279-139,974,382 UAP1L1
    nsv5492009copy number variation1nstd206human GRCh38 chr9: 137,079,827-137,079,931 , GRCh37.p13 chr9: 139,974,279-139,974,383 UAP1L1
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5381736copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,764,148-141,066,491 , GRCh38.p12 chr9: 136,869,696-138,172,039 PTGDS, LCN12, 63 more genes
    nsv5243007copy number variation1nstd204human GRCh38.p13 chr9: 136,845,001-137,273,000 , GRCh37.p13 chr9: 139,739,453-140,167,452 ENTPD2, LINC02908, 43 more genes
    nsv4985882copy number variation1nstd200human GRCh38 chr9: 137,077,923-137,094,783 , GRCh37.p13 chr9: 139,972,375-139,989,235 MAN1B1-DT, UAP1L1, 1 more genes
    nsv4768352copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532 MIR6722, EXD3, 108 more genes
    nsv4728942copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,776,707-140,234,193 , GRCh38.p12 chr9: 136,882,255-137,339,741 GRIN1, CYSRT1, 42 more genes
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv4683252copy number variation2nstd102humanUncertain significance GRCh37 chr9: 138,594,085-140,062,314 , GRCh38.p12 chr9: 135,702,239-137,167,862 SAPCD2, MIR3621, 81 more genes
    nsv4681206copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,645,763-140,729,425 , GRCh38.p12 chr9: 135,753,917-137,834,973 DPP7, MIR4673, 112 more genes
    nsv4614420copy number variation1nstd183human GRCh37 chr9: 139,964,308-139,972,012 , GRCh38.p12 chr9: 137,069,856-137,077,560 SAPCD2, UAP1L1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456509copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,766,260-140,186,072 , GRCh38.p12 chr9: 136,871,808-137,291,620 PAXX, CIMIP2A, 40 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4383485copy number variation1nstd173human GRCh37 chr9: 139,059,275-140,803,861 , GRCh38.p12 chr9: 136,167,429-137,909,409 , LRRC26, 107 more genes
    nsv4367274copy number variation1nstd173human GRCh37 chr9: 139,563,040-140,180,735 , GRCh38.p12 chr9: 136,668,588-137,286,283 , LCN10, 67 more genes
    nsv4185317copy number variation1nstd166human GRCh37.p13 chr9: 139,974,276-139,974,383 , GRCh38.p12 chr9: 137,079,824-137,079,931 UAP1L1
    nsv4178974copy number variation1nstd166human GRCh37.p13 chr9: 139,970,437-139,986,039 , GRCh38.p12 chr9: 137,075,985-137,091,587 MAN1B1-DT, MAN1B1, 1 more genes
    nsv3969894insertion1nstd168human GRCh38 chr9: 137,073,039-137,130,059 , GRCh37.p13 chr9: 139,967,491-140,024,511 , MAN1B1, 3 more genes
    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