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 259

    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
    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
    nsv6976703copy number variation1nstd229human GRCh38 chr15: 93,071,758-93,072,555 , GRCh37.p13 chr15: 93,614,987-93,615,784 RGMA
    nsv6971501copy number variation1nstd229human GRCh38 chr15: 93,029,301-93,036,000 , GRCh37.p13 chr15: 93,572,531-93,579,230 RGMA
    nsv6971371copy number variation1nstd229human GRCh38 chr15: 93,060,736-93,063,327 , GRCh37.p13 chr15: 93,603,965-93,606,556 RGMA, YBX2P2
    nsv6970630copy number variation1nstd229human GRCh38 chr15: 93,023,391-93,614,022 , GRCh37.p13 chr15: 93,566,621-94,157,251 LOC101927025, LOC107983974, 6 more genes
    nsv6970046copy number variation1nstd229human GRCh38 chr15: 92,740,860-93,077,278 , GRCh37.p13 chr15: 93,284,090-93,620,507 CHASERR, MIR3175, 6 more genes
    nsv6968895copy number variation1nstd229human GRCh38 chr15: 93,046,794-93,046,869 , GRCh37.p13 chr15: 93,590,024-93,590,099 RGMA
    nsv6965956copy number variation1nstd229human GRCh38 chr15: 93,028,001-93,046,500 , GRCh37.p13 chr15: 93,571,231-93,589,730 RGMA, CHD2
    nsv6963888copy number variation1nstd229human GRCh38 chr15: 92,996,407-93,107,043 , GRCh37.p13 chr15: 93,539,637-93,650,272 RGMA, YBX2P2, 2 more genes
    nsv6963577copy number variation1nstd229human GRCh38 chr15: 92,978,516-93,047,446 , GRCh37.p13 chr15: 93,521,746-93,590,676 RGMA, CHD2
    nsv6961417copy number variation1nstd229human GRCh38 chr15: 92,981,553-93,187,550 , GRCh37.p13 chr15: 93,524,783-93,730,779 YBX2P2, CHD2, 2 more genes
    nsv6959116copy number variation1nstd229human GRCh38 chr15: 92,964,473-93,499,724 , GRCh37.p13 chr15: 93,507,703-94,042,953 LOC105370982, CHD2, 5 more genes
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6505925copy number variation1nstd223human GRCh38 chr15: 93,027,921-93,046,540 , GRCh37.p13 chr15: 93,571,151-93,589,770 CHD2, RGMA
    nsv6291795copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262 LINC00930, TRY-GTA12-1, 106 more genes
    nsv6290316copy number variation1nstd102humanPathogenic GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617 LOC105370964, MRPL46, 130 more genes
    nsv6203718copy number variation1nstd214human GRCh38 chr15: 93,046,794-93,046,868 , GRCh37.p13 chr15: 93,590,024-93,590,098 RGMA
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
    nsv6132919copy number variation1nstd213human GRCh37 chr15: 91,580,000-100,660,001 , GRCh38.p12 chr15: 91,036,770-100,119,796 ST8SIA2, SYNM, 116 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