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 589

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7097932copy number variation1nstd102humanUncertain significance GRCh37 chr9: 133,884,602-135,942,612 , GRCh38.p12 chr9: 131,009,215-133,067,225 LAMC3, SPACA9, 40 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7074813inversion1nstd229human GRCh38 chr9: 131,941,625-131,947,401 , GRCh37.p13 chr9: 134,817,012-134,822,788 MED27
    nsv7072680inversion1nstd229human GRCh38 chr9: 131,878,307-131,878,328 , GRCh37.p13 chr9: 134,753,694-134,753,715 MED27
    nsv7070528inversion1nstd229human GRCh38 chr9: 131,936,612-131,947,680 , GRCh37.p13 chr9: 134,811,999-134,823,067 MED27
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6877738copy number variation1nstd229human GRCh38 chr9: 132,019,654-132,024,278 , GRCh37.p13 chr9: 134,895,041-134,899,665 MED27
    nsv6876254copy number variation1nstd229human GRCh38 chr9: 132,038,695-132,039,710 , GRCh37.p13 chr9: 134,914,082-134,915,097 MED27
    nsv6874915copy number variation1nstd229human GRCh38 chr9: 131,951,478-131,956,421 , GRCh37.p13 chr9: 134,826,865-134,831,808 MED27
    nsv6874451copy number variation1nstd229human GRCh38 chr9: 131,872,535-131,872,720 , GRCh37.p13 chr9: 134,747,922-134,748,107 MED27
    nsv6874310copy number variation1nstd229human GRCh38 chr9: 131,915,632-131,942,322 , GRCh37.p13 chr9: 134,791,019-134,817,709 MED27
    nsv6874073copy number variation1nstd229human GRCh38 chr9: 131,901,709-131,952,575 , GRCh37.p13 chr9: 134,777,096-134,827,962 MED27
    nsv6873449copy number variation1nstd229human GRCh38 chr9: 131,884,301-131,885,900 , GRCh37.p13 chr9: 134,759,688-134,761,287 MED27
    nsv6873419copy number variation1nstd229human GRCh38 chr9: 131,979,461-132,051,719 , GRCh37.p13 chr9: 134,854,848-134,927,106 MED27
    nsv6872543copy number variation1nstd229human GRCh38 chr9: 132,059,563-132,066,791 , GRCh37.p13 chr9: 134,934,950-134,942,178 MED27
    nsv6872445copy number variation1nstd229human GRCh38 chr9: 132,025,201-132,030,100 , GRCh37.p13 chr9: 134,900,588-134,905,487 MED27
    nsv6871929copy number variation1nstd229human GRCh38 chr9: 131,990,695-131,998,272 , GRCh37.p13 chr9: 134,866,082-134,873,659 MED27
    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