U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 893

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2667872copy number variation147estd199human GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952 DNAH14
    esv2676574copy number variation189estd199human GRCh37 chr6: 78,967,194-79,036,497 , GRCh38.p12 chr6: 78,257,477-78,326,780 LOC105377865
    esv2670203copy number variation158estd199human GRCh37 chr6: 78,967,194-79,036,475 , GRCh38.p12 chr6: 78,257,477-78,326,758 LOC105377865
    esv2668226copy number variation311estd199human GRCh37 chr3: 129,763,245-129,799,692 , GRCh38.p12 chr3: 130,044,402-130,080,849 ALG1L2
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2665317copy number variation65estd199human GRCh37 chr11: 7,811,173-7,833,378 , GRCh38.p12 chr11: 7,789,626-7,811,831 , GRCh38.p12 chr11|NT_187583.1: 10,494-32,699 , GRCh38.p12 chr11|NW_011332695.1: 10,494-32,701 OR5P2
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2663133copy number variation46estd199human GRCh37 chr6: 32,629,745-32,648,392 , GRCh38.p12 chr6: 32,661,968-32,680,615 HLA-DQB1
    esv2669960copy number variation208estd199human GRCh37 chr9: 41,968,745-41,984,492 , GRCh38.p12 chr9: 39,823,727-39,839,474 FGF7P3
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2668861copy number variation64estd199human GRCh37 chr9: 6,700,452-6,710,572 , GRCh38.p12 chr9: 6,700,452-6,710,572 LINC02851
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2677090copy number variation28estd199human GRCh37 chr9: 6,701,595-6,711,642 , GRCh38.p12 chr9: 6,701,595-6,711,642 LINC02851
    esv2675979copy number variation520estd199human GRCh37 chr6: 53,924,803-53,934,828 , GRCh38.p12 chr6: 54,060,005-54,070,030 MLIP
    esv2661768copy number variation445estd199human GRCh37 chr5: 12,811,019-12,820,535 , GRCh38.p12 chr5: 12,810,907-12,820,423 LOC105374657
    esv2673043copy number variation328estd199human GRCh37 chr14: 80,106,288-80,115,049 , GRCh38.p12 chr14: 79,639,945-79,648,706 NRXN3
    esv2676043copy number variation92estd199human GRCh37 chr3: 37,978,417-37,986,927 , GRCh38.p12 chr3: 37,936,926-37,945,436 CTDSPL
    esv2677597copy number variation57estd199human GRCh37 chr15: 100,414,545-100,422,992 , GRCh38.p12 chr15: 99,874,340-99,882,787 LOC400464
    esv2659844copy number variation372estd199human GRCh37 chr6: 53,925,724-53,934,162 , GRCh38.p12 chr6: 54,060,926-54,069,364 MLIP
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    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