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 154

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7074617inversion1nstd229human GRCh38 chr10: 86,025,751-89,446,782 , GRCh37.p13 chr10: 87,785,508-91,206,539 GRID1, LDB3, 83 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6898040copy number variation1nstd229human GRCh38 chr10: 89,201,122-89,204,210 , GRCh37.p13 chr10: 90,960,879-90,963,967 LOC105378418, CH25H
    nsv6895451copy number variation1nstd229human GRCh38 chr10: 89,199,701-89,233,000 , GRCh37.p13 chr10: 90,959,458-90,992,757 LOC105378418, CH25H, 1 more genes
    nsv6883820copy number variation1nstd229human GRCh38 chr10: 89,203,984-89,204,697 , GRCh37.p13 chr10: 90,963,741-90,964,454 CH25H, LOC105378418
    nsv6883259copy number variation1nstd229human GRCh38 chr10: 88,909,886-89,428,064 , GRCh37.p13 chr10: 90,669,643-91,187,821 IFIT2, STAMBPL1, 18 more genes
    nsv6883010copy number variation1nstd229human GRCh38 chr10: 89,085,834-89,335,959 , GRCh37.p13 chr10: 90,845,591-91,095,716 IFIT2, CH25H, 6 more genes
    nsv6878566copy number variation1nstd229human GRCh38 chr10: 89,202,450-89,217,741 , GRCh37.p13 chr10: 90,962,207-90,977,498 LOC105378418, CH25H, 1 more genes
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637707copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,672,265-91,165,763 , GRCh38.p12 chr10: 88,912,508-89,406,006 IFIT1, IFIT3, 16 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6637182copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,874,051-91,291,188 , GRCh38.p12 chr10: 89,114,294-89,531,431 IFIT5, IFIT6P, 13 more genes
    nsv6634458copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320 IFIT5, IFIT1, 140 more genes
    nsv6453718copy number variation1nstd223human GRCh38 chr10: 89,199,672-89,232,976 , GRCh37.p13 chr10: 90,959,429-90,992,733 CH25H, LIPA, 1 more genes
    nsv6452128copy number variation1nstd223human GRCh38 chr10: 89,202,450-89,217,738 , GRCh37.p13 chr10: 90,962,207-90,977,495 LOC105378418, CH25H, 1 more genes
    nsv6440748copy number variation1nstd223human GRCh38 chr10: 89,203,984-89,204,697 , GRCh37.p13 chr10: 90,963,741-90,964,454 LOC105378418, CH25H
    nsv6309171copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,694,970-91,007,415 , GRCh38.p12 chr10: 88,935,213-89,247,658 FAS-AS1, LOC100289238, 8 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