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 420

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7137114copy number variation1nstd102humanPathogenic GRCh37 chr15: 98,996,113-101,211,899 , GRCh38.p12 chr15: 98,452,884-100,671,694 PGPEP1L, LOC105371017, 36 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7074837inversion1nstd229human GRCh38 chr15: 98,618,777-101,109,346 , GRCh37.p13 chr15: 99,162,006-101,649,551 LOC440313, PRKXP1, 42 more genes
    nsv7065629inversion1nstd229human GRCh38 chr15: 99,118,517-99,123,821 , GRCh37.p13 chr15: 99,658,722-99,664,026 , GRCh37.p13 chr15|NW_003871084.1: 32,020-37,324 SYNM
    nsv7065226inversion1nstd229human GRCh38 chr15: 98,338,625-100,843,802 , GRCh37.p13 chr15: 98,881,854-101,384,007 LOC102723335, LUNAR1, 39 more genes
    nsv7064824inversion1nstd229human GRCh38 chr15: 98,981,210-99,387,289 , GRCh37.p13 chr15: 99,524,439-99,927,494 SYNM-AS1, TTC23, 6 more genes
    nsv7063694inversion1nstd229human GRCh38 chr15: 98,738,473-100,284,229 , GRCh37.p13 chr15: 99,281,702-100,824,434 MIR4714, PGPEP1L, 22 more genes
    nsv6977811copy number variation1nstd229human GRCh38 chr15: 99,129,378-99,133,071 , GRCh37.p13 chr15|NW_003871084.1: 22,770-26,463 , GRCh37.p13 chr15: 99,669,583-99,673,276 SYNM
    nsv6977137copy number variation1nstd229human GRCh38 chr15: 98,919,969-99,497,854 , GRCh37.p13 chr15: 99,463,198-100,038,059 SYNM, LINC02244, 11 more genes
    nsv6977108copy number variation1nstd229human GRCh38 chr15: 99,120,901-99,125,300 , GRCh37.p13 chr15|NW_003871084.1: 30,541-34,940 , GRCh37.p13 chr15: 99,661,106-99,665,505 SYNM
    nsv6975600copy number variation1nstd229human GRCh38 chr15: 98,893,001-99,187,900 , GRCh37.p13 chr15|NW_003871084.1: 1-170,033 , GRCh37.p13 chr15: 99,436,230-99,728,105 IGF1R, PGPEP1L, 4 more genes
    nsv6972045copy number variation1nstd229human GRCh38 chr15: 98,854,051-99,246,000 , GRCh37.p13 chr15: 99,397,280-99,786,205 IGF1R, SYNM-AS1, 4 more genes
    nsv6971840copy number variation1nstd229human GRCh38 chr15: 99,118,781-99,121,206 , GRCh37.p13 chr15|NW_003871084.1: 34,635-37,060 , GRCh37.p13 chr15: 99,658,986-99,661,411 SYNM
    nsv6969731copy number variation1nstd229human GRCh38 chr15: 99,110,123-99,131,972 , GRCh37.p13 chr15: 99,650,328-99,672,177 , GRCh37.p13 chr15|NW_003871084.1: 23,869-45,718 SYNM
    nsv6969669copy number variation1nstd229human GRCh38 chr15: 99,072,984-99,466,581 , GRCh37.p13 chr15: 99,696,046-100,006,786 SYNM-AS1, TTC23, 6 more genes
    nsv6967448copy number variation1nstd229human GRCh38 chr15: 99,136,860-99,140,269 , GRCh37.p13 chr15|NW_003871084.1: 15,572-18,981 , GRCh37.p13 chr15: 99,677,065-99,680,474 SYNM, TTC23
    nsv6964306copy number variation1nstd229human GRCh38 chr15: 99,083,504-99,558,228 , GRCh37.p13 chr15: 99,696,046-100,098,433 LRRC28, LOC105371017, 9 more genes
    nsv6964225copy number variation1nstd229human GRCh38 chr15: 99,025,601-99,129,800 , GRCh37.p13 chr15: 99,568,830-99,670,005 , GRCh37.p13 chr15|NW_003871084.1: 26,041-130,240 SYNM-AS1, SYNM, 1 more genes
    nsv6963195copy number variation1nstd229human GRCh38 chr15: 98,972,725-99,619,452 , GRCh37.p13 chr15: 99,515,954-100,159,657 LRRC28, LOC105371017, 12 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