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 1431

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2674484copy number variation82estd199human GRCh37 chr1: 225,133,646-225,248,670 , GRCh38.p12 chr1: 224,945,944-225,060,968 DNAH14
    esv2673642copy number variation50estd199human GRCh37 chrX: 91,853,345-91,909,992 , GRCh38.p12 chrX: 92,598,346-92,654,993 PCDH11X
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2657875copy number variation20estd199human GRCh37 chr7: 6,120,895-6,145,442 , GRCh38.p12 chr7: 6,081,264-6,105,811 USP42
    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
    esv2668941copy number variation11estd199human GRCh37 chr7: 34,895,752-34,913,775 , GRCh38.p12 chr7: 34,856,140-34,874,163 NPSR1
    esv2674710copy number variation1estd199human GRCh37 chr8: 64,835,565-64,851,633 , GRCh38.p12 chr8: 63,923,008-63,939,076 LINC01414
    esv2676907copy number variation19estd199human GRCh37 chr5: 155,577,191-155,591,407 , GRCh38.p12 chr5: 156,150,181-156,164,397 SGCD
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2670295copy number variation118estd199human GRCh37 chr3: 114,656,952-114,668,601 , GRCh38.p12 chr3: 114,938,105-114,949,754 ZBTB20
    esv2677965copy number variation40estd199human GRCh37 chr4: 92,073,713-92,084,451 , GRCh38.p12 chr4: 91,152,562-91,163,300 CCSER1
    esv2660593copy number variation56estd199human GRCh37 chrX: 91,610,345-91,620,792 , GRCh38.p12 chrX: 92,355,346-92,365,793 PCDH11X
    esv2672284copy number variation80estd199human GRCh37 chr11: 107,233,995-107,244,392 , GRCh38.p12 chr11: 107,363,269-107,373,666 CWF19L2
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2670098copy number variation35estd199human GRCh37 chr16: 76,661,500-76,671,078 , GRCh38.p12 chr16: 76,627,603-76,637,181 LINC02125
    esv2658746copy number variation20estd199human GRCh37 chr15: 76,336,512-76,346,064 , GRCh38.p12 chr15: 76,044,171-76,053,723 NRG4
    esv2657507copy number variation27estd199human GRCh37 chr1: 10,369,469-10,378,666 , GRCh38.p12 chr1: 10,309,411-10,318,608 KIF1B
    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