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 191

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv5694681mobile element insertion2nstd211human GRCh38 chr15: 92,881,576-92,881,576 , GRCh37.p13 chr15: 93,424,806-93,424,806 CHASERR
    nsv5531067copy number variation1nstd206human GRCh38 chr15: 92,402,520-97,547,707 , GRCh37.p13 chr15: 92,945,750-98,090,937 , LOC105371004, 71 more genes
    nsv5419274mobile element insertion1nstd206human GRCh38 chr15: 92,881,576-92,881,627 , GRCh37.p13 chr15: 93,424,806-93,424,857 CHASERR
    nsv5272015copy number variation1nstd204human GRCh38.p13 chr15: 92,883,601-92,941,000 , GRCh37.p13 chr15: 93,426,831-93,484,230 MIR3175, CHASERR, 1 more genes
    nsv5262208copy number variation1nstd204human GRCh38.p13 chr15: 92,864,001-92,882,600 , GRCh37.p13 chr15: 93,407,231-93,425,830 CHASERR
    nsv5143785mobile element insertion1nstd203human GRCh38 chr15: 92,881,562-92,881,576 , GRCh37.p13 chr15: 93,424,792-93,424,806 CHASERR
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 CHD2, MIR11181, 272 more genes
    nsv4728945copy number variation1nstd102humanUncertain significance GRCh37 chr15: 93,392,804-93,540,230 , GRCh38.p12 chr15: 92,849,574-92,997,000 CHASERR, MIR3175, 1 more genes
    nsv4675851copy number variation1nstd102humanUncertain significance GRCh37 chr15: 93,373,121-93,747,449 , GRCh38.p12 chr15: 92,829,891-93,204,220 CHD2, YBX2P2, 5 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 TTLL13, LINC00052, 264 more genes
    nsv4619075copy number variation1nstd183human GRCh37 chr15: 93,422,215-93,467,232 , GRCh38.p12 chr15: 92,878,985-92,924,002 CHD2, MIR3175, 1 more genes
    nsv4506952mobile element insertion1nstd166human GRCh37.p13 chr15: 93,424,792-93,424,792 , GRCh38.p12 chr15: 92,881,562-92,881,562 CHASERR
    nsv4506080mobile element insertion1nstd166human GRCh37.p13 chr15: 93,439,782-93,439,782 , GRCh38.p12 chr15: 92,896,552-92,896,552 CHASERR
    nsv4456778copy number variation1nstd102humanPathogenic GRCh37 chr15: 91,229,877-93,677,014 , GRCh38.p12 chr15: 90,686,646-93,133,785 H2AZ2P1, MAN2A2, 44 more genes
    nsv4456430copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,288,175-102,429,112 , GRCh38.p12 chr15: 89,744,944-101,888,909 IQGAP1, LOC400464, 210 more genes
    nsv4432278copy number variation1nstd172human GRCh38.p12 chr15: 92,879,771-92,915,770 , GRCh37.p13 chr15: 93,423,001-93,459,000 CHD2, MIR3175, 1 more genes
    nsv4377776copy number variation1nstd173human GRCh37 chr15: 86,980,083-93,499,239 , GRCh38.p12 chr15: 86,436,852-92,956,009 , RNU6-1111P, 136 more genes
    nsv4251512copy number variation1nstd166human GRCh37.p13 chr15: 93,423,000-93,428,000 , GRCh38.p12 chr15: 92,879,770-92,884,770 CHASERR
    nsv3923433copy number variation1nstd102humanUncertain significance NCBI36 chr15: 91,097,827-91,321,397 , GRCh37.p13 chr15: 93,296,823-93,520,393 , GRCh38.p12 chr15: 92,753,593-92,977,163 CHD2, MIR3175, 4 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