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 190

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5712780mobile element insertion2nstd211human GRCh38 chr10: 125,816,870-125,816,870 , GRCh37.p13 chr10: 127,505,439-127,505,439 UROS
    nsv5506299copy number variation1nstd206human GRCh38 chr10: 125,790,607-125,790,889 , GRCh37.p13 chr10: 127,479,176-127,479,458 UROS
    nsv5404942mobile element insertion1nstd206human GRCh38 chr10: 125,816,870-125,816,921 , GRCh37.p13 chr10: 127,505,439-127,505,490 UROS
    nsv5364894translocation1nstd200human GRCh38 chr10: 125,803,490-125,803,490 , GRCh38 chr10: 43,420,582-43,420,582 , GRCh37.p13 chr10: 43,916,030-43,916,030 , GRCh37.p13 chr10: 127,492,059-127,492,059 UROS
    nsv5341002translocation1nstd200human GRCh37 chr10: 127,492,059-127,492,059 , GRCh37 chr10: 43,916,030-43,916,030 , GRCh38.p12 chr10: 43,420,582-43,420,582 , GRCh38.p12 chr10: 125,803,490-125,803,490 UROS
    nsv4983971copy number variation1nstd200human GRCh38 chr10: 125,039,754-126,334,238 , GRCh37.p13 chr10: 126,728,323-128,022,807 , ADAM12, 28 more genes
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4610879copy number variation1nstd183human GRCh37 chr10: 127,459,480-127,491,165 , GRCh38.p12 chr10: 125,770,911-125,802,596 MMP21, UROS
    nsv4527816copy number variation1nstd166human GRCh37.p13 chr10: 127,512,324-127,512,391 , GRCh38.p12 chr10: 125,823,755-125,823,822 UROS, BCCIP
    nsv4497965mobile element insertion1nstd166human GRCh37.p13 chr10: 127,505,426-127,505,426 , GRCh38.p12 chr10: 125,816,857-125,816,857 UROS
    nsv4456733copy number variation1nstd102humanPathogenic GRCh37 chr10: 124,988,334-135,427,143 , GRCh38.p12 chr10: 123,228,818-133,613,639 FAM53B-AS1, LOC105378544, 153 more genes
    nsv4456626copy number variation1nstd102humanPathogenic GRCh37 chr10: 114,544,537-135,427,143 , GRCh38.p12 chr10: 112,784,778-133,613,639 LOC105378521, ZRANB1, 317 more genes
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
    nsv4210066copy number variation1nstd166human GRCh37.p13 chr10: 127,476,327-127,477,275 , GRCh38.p12 chr10: 125,787,758-125,788,706 UROS
    nsv4207485copy number variation1nstd166human GRCh37.p13 chr10: 127,504,547-127,512,390 , GRCh38.p12 chr10: 125,815,978-125,823,821 MIR4484, UROS, 1 more genes
    nsv3924720copy number variation1nstd102humanPathogenic GRCh38 chr10: 119,707,856-133,613,639 , GRCh37 chr10: 121,467,368-135,427,143 , NCBI36 chr10: 121,457,358-135,277,133 OR6L2P, RPL19P16, 208 more genes
    nsv3923859copy number variation1nstd102humanPathogenic NCBI36 chr10: 113,062,847-135,284,168 , GRCh37 chr10: 113,072,857-135,434,178 , GRCh38 chr10: 111,313,099-133,620,674 AS-PTPRE, SFXN4, 330 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 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