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 186

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5488682copy number variation1nstd206human GRCh38 chr9: 129,807,303-129,814,738 , GRCh37.p13 chr9: 132,569,582-132,577,017 TOR1A, TOR1B
    nsv5483905copy number variation1nstd206human GRCh38 chr9: 129,698,067-130,033,998 , GRCh37.p13 chr9: 132,460,346-132,796,277 MIR6855, PRRX2, 8 more genes
    nsv5379532translocation1nstd200human GRCh38 chr9: 129,820,589-129,820,589 , GRCh38 chr9: 129,607,011-129,607,011 , GRCh37.p13 chr9: 132,369,290-132,369,290 , GRCh37.p13 chr9: 132,582,868-132,582,868 TOR1A, NTMT1
    nsv5250774copy number variation1nstd204human GRCh38.p13 chr9: 129,443,501-129,853,600 , GRCh37.p13 chr9: 132,205,780-132,615,879 ASB6, C9orf50, 12 more genes
    nsv5246717copy number variation1nstd204human GRCh37.p13 chr9: 132,524,680-132,876,179 , GRCh38.p13 chr9: 129,762,401-130,113,900 TOR1A, USP20, 6 more genes
    nsv4988474copy number variation1nstd200human GRCh38 chr9: 129,810,827-129,811,438 , GRCh37.p13 chr9: 132,573,106-132,573,717 TOR1B, TOR1A
    nsv4836919copy number variation1nstd200human GRCh37 chr9: 132,573,106-132,573,717 , GRCh38.p12 chr9: 129,810,827-129,811,438 TOR1A, TOR1B
    nsv4729432copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,470,092-133,044,256 , GRCh38.p12 chr9: 129,707,813-130,281,977 GPRACR, NCS1, 13 more genes
    nsv4729206copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,448,018-132,581,300 , GRCh38.p12 chr9: 129,685,739-129,819,021 PTGES, PRRX2-AS1, 4 more genes
    nsv4675061copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,449,936-132,795,093 , GRCh38.p12 chr9: 129,687,657-130,032,814 TOR1A, PRRX2, 8 more genes
    nsv4663874copy number variation1nstd186human GRCh37 chr9: 132,463,983-132,648,102 , GRCh38.p12 chr9: 129,701,704-129,885,823 C9orf78, PRRX2, 8 more genes
    nsv4653496copy number variation1nstd186human GRCh37 chr9: 132,463,983-132,648,102 , GRCh38.p12 chr9: 129,701,704-129,885,823 FNBP1, TOR1B, 8 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456688copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,183,626-133,431,092 , GRCh38.p12 chr9: 129,421,347-130,555,705 ASB6, GPR107, 22 more genes
    nsv4455331copy number variation1nstd102humanUncertain significance GRCh37 chr9: 132,449,921-132,793,004 , GRCh38.p12 chr9: 129,687,642-130,030,725 UBE2V1P4, MIR6855, 8 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
    nsv4367225copy number variation1nstd173human GRCh37 chr9: 132,449,937-132,582,750 , GRCh38.p12 chr9: 129,687,658-129,820,471 UBE2V1P4, PTGES, 4 more genes
    nsv4349353copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 131,670,024-134,514,071 , GRCh38.p12 chr9: 128,907,745-131,638,684 ABL1, ASS1, 69 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4192028copy number variation1nstd166human GRCh37.p13 chr9: 132,583,513-132,584,176 , GRCh38.p12 chr9: 129,821,234-129,821,897 TOR1A
    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