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 124

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112709copy number variation1nstd102humanPathogenic GRCh37 chr3: 123,000,000-129,700,000 , GRCh38.p12 chr3: 123,281,153-129,981,157 OR7E97P, MARK3P3, 160 more genes
    nsv6112688copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,154,188-128,324,987 , GRCh38.p12 chr3: 120,435,341-128,606,144 RNU4-62P, MTCO1P29, 169 more genes
    nsv5957309insertion1nstd209human GRCh38 chr3: 123,986,018-123,986,018 , GRCh37.p13 chr3: 123,704,865-123,704,865 ROPN1
    nsv5891384copy number variation1nstd209human GRCh38 chr3: 123,983,308-123,983,357 , GRCh37.p13 chr3: 123,702,155-123,702,204 ROPN1
    nsv5730287mobile element insertion1nstd211human GRCh38 chr3: 123,970,728-123,970,728 , GRCh37.p13 chr3: 123,689,575-123,689,575 ROPN1
    nsv5582469copy number variation1nstd207human GRCh38 chr3: 123,981,979-123,990,770 , GRCh37.p13 chr3: 123,700,826-123,709,617 ROPN1
    nsv5447848copy number variation1nstd206human GRCh38 chr3: 123,957,708-124,017,823 , GRCh37.p13 chr3: 123,676,555-123,736,670 CCDC14, ROPN1
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4804798copy number variation1nstd200human GRCh37 chr3: 123,625,351-123,799,129 , GRCh38.p12 chr3: 123,906,504-124,080,282 KALRN, CCDC14, 1 more genes
    nsv4728210copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,442,360-123,837,654 , GRCh38.p12 chr3: 123,723,513-124,118,807 MYLK, KALRN, 2 more genes
    nsv4674011copy number variation1nstd102humanUncertain significance GRCh37 chr3: 122,981,355-123,768,908 , GRCh38.p12 chr3: 123,262,508-124,050,061 ROPN1, LOC105369194, 8 more genes
    nsv4587199copy number variation1nstd183human GRCh37 chr3: 123,704,976-123,720,217 , GRCh38.p12 chr3: 123,986,129-124,001,370 ROPN1
    nsv4468940mobile element insertion1nstd166human GRCh37.p13 chr3: 123,690,861-123,690,861 , GRCh38.p12 chr3: 123,972,014-123,972,014 ROPN1
    nsv3924082copy number variation1nstd102humanPathogenic NCBI36 chr3: 119,875,435-127,742,263 , GRCh38 chr3: 118,673,898-126,540,730 , GRCh37 chr3: 118,392,745-126,259,573 MYLK-AS2, RPL7AP11, 165 more genes
    nsv3923097copy number variation1nstd102humanPathogenic NCBI36 chr3: 120,318,703-127,122,267 , GRCh38 chr3: 119,117,166-125,920,734 , GRCh37 chr3: 118,836,013-125,639,577 POGLUT1, RN7SL397P, 141 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3919464copy number variation1nstd102humanPathogenic GRCh38 chr3: 114,122,562-124,532,374 , GRCh37 chr3: 113,841,409-124,251,221 , NCBI36 chr3: 115,324,099-125,733,911 B4GALT4-AS1, LSAMP, 144 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918094copy number variation1nstd102humanPathogenic NCBI36 chr3: 113,822,514-129,935,667 , GRCh38 chr3: 112,620,977-128,734,134 , GRCh37 chr3: 112,339,824-128,452,977 QTRT2, MIR544B, 284 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