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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3110178copy number variation1nstd145human GRCh37 chr4: 5,243,210-5,390,044 , GRCh38.p12 chr4: 5,241,483-5,388,317 STK32B
    nsv3117986copy number variation2nstd145human GRCh37 chr4: 70,182,214-70,227,164 , GRCh38.p12 chr4: 69,316,496-69,361,446 LOC642496
    nsv3113267copy number variation16nstd145human GRCh37 chr20: 1,561,593-1,593,574 , GRCh38.p12 chr20: 1,580,947-1,612,928 SIRPB1
    nsv3111358copy number variation1nstd145human GRCh37 chr9: 28,315,953-28,347,594 , GRCh38.p12 chr9: 28,315,955-28,347,596 LINGO2
    nsv3114057copy number variation160nstd145human GRCh37 chr19: 52,134,789-52,148,550 , GRCh38.p12 chr19: 51,631,536-51,645,297 SIGLEC14
    nsv3111733copy number variation53nstd145human GRCh37 chr1: 169,227,837-169,240,805 , GRCh38.p12 chr1: 169,258,599-169,271,567 NME7
    nsv3110942copy number variation60nstd145human GRCh37 chr7: 91,033,585-91,042,496 , GRCh38.p12 chr7: 91,404,270-91,413,181 LINC02932
    nsv3112700copy number variation32nstd145human GRCh37 chr12: 86,695,674-86,703,013 , GRCh38.p12 chr12: 86,301,896-86,309,235 MGAT4C
    nsv3110514copy number variation75nstd145human GRCh37 chr8: 51,031,100-51,038,303 , GRCh38.p12 chr8: 50,118,540-50,125,743 SNTG1
    nsv3110125copy number variation1nstd145human GRCh37 chr9: 28,826,833-28,834,032 , GRCh38.p12 chr9: 28,826,835-28,834,034 LINGO2
    nsv3117305copy number variation1nstd145human GRCh37 chr22: 35,842,170-35,848,481 , GRCh38.p12 chr22: 35,446,177-35,452,488 MCM5
    nsv3112629copy number variation2nstd145human GRCh37 chr12: 68,442,913-68,447,752 , GRCh38.p12 chr12: 68,049,133-68,053,972
    nsv3115871copy number variation21nstd145human GRCh37 chr11: 99,647,381-99,652,155 , GRCh38.p12 chr11: 99,776,650-99,781,424 CNTN5
    nsv3112046copy number variation55nstd145human GRCh37 chr19: 54,556,015-54,560,055 , GRCh38.p12 chr19: 54,052,761-54,056,801 , GRCh38.p12 chr19|NT_187693.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571061.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571057.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571058.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571059.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571060.1: 27,128-31,168 , GRCh38.p12 chr19|NW_003571056.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571055.2: 27,128-31,168 , GRCh38.p12 chr19|NW_003571054.1: 27,128-31,168 VSTM1
    nsv3117571copy number variation81nstd145human GRCh37 chr11: 107,239,191-107,242,941 , GRCh38.p12 chr11: 107,368,465-107,372,215 CWF19L2
    nsv3114982copy number variation1nstd145human GRCh37 chr11: 5,797,551-5,801,095 , GRCh38.p12 chr11: 5,776,321-5,779,865 OR52N5
    nsv3115580copy number variation4nstd145human GRCh37 chr6: 122,156,421-122,159,429 , GRCh38.p12 chr6: 121,835,275-121,838,283 LOC105377979
    nsv3114005copy number variation35nstd145human GRCh37 chr22: 37,144,978-37,146,950 , GRCh38.p12 chr22: 36,748,934-36,750,906 CACNG2-DT
    nsv3114312copy number variation223nstd145human GRCh37 chr2: 76,773,866-76,775,310 , GRCh38.p12 chr2: 76,546,740-76,548,184 LOC105374814
    nsv3112092copy number variation1nstd145human GRCh37 chr17: 80,940,622-80,993,541 , GRCh38.p12 chr17: 82,982,746-83,035,665 , GRCh38.p12 chr17|NT_187612.1: 66,811-118,712 B3GNTL1
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