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 115

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5393461mobile element deletion1nstd186human GRCh37 chr1: 25,158,703-25,161,509 , GRCh38.p12 chr1: 24,832,212-24,835,018 CLIC4
    nsv5393597mobile element deletion2nstd186human GRCh37 chr2: 202,146,658-202,149,440 , GRCh38.p12 chr2: 201,281,935-201,284,717 CASP8
    nsv5393645mobile element deletion2nstd186human GRCh37 chr12: 96,233,592-96,236,327 , GRCh38.p12 chr12: 95,839,814-95,842,549 SNRPF-DT
    nsv5393809mobile element deletion1nstd186human GRCh37 chr3: 128,672,376-128,675,101 , GRCh38.p12 chr3: 128,953,533-128,956,258 CFAP92
    nsv5393527mobile element deletion1nstd186human GRCh37 chr10: 32,257,895-32,260,612 , GRCh38.p12 chr10: 31,968,967-31,971,684 LOC107984219
    nsv5393599mobile element deletion1nstd186human GRCh37 chr12: 70,594,864-70,597,577 , GRCh38.p12 chr12: 70,201,084-70,203,797 LINC02821
    nsv5393505mobile element deletion1nstd186human GRCh37 chr3: 128,672,376-128,675,076 , GRCh38.p12 chr3: 128,953,533-128,956,233 CFAP92
    nsv5393540mobile element deletion1nstd186human GRCh37 chr12: 96,340,356-96,343,001 , GRCh38.p12 chr12: 95,946,578-95,949,223 AMDHD1
    nsv5393887mobile element deletion1nstd186human GRCh37 chr6: 29,685,488-29,688,101 , GRCh38.p12 chr6: 29,717,711-29,720,324 HCG4P11
    nsv5393615mobile element deletion2nstd186human GRCh37 chr7: 100,337,915-100,340,524 , GRCh38.p12 chr7: 100,740,292-100,742,901 ZAN
    nsv5393494mobile element deletion1nstd186human GRCh37 chr12: 96,340,355-96,342,954 , GRCh38.p12 chr12: 95,946,577-95,949,176 AMDHD1
    nsv5393700mobile element deletion2nstd186human GRCh37 chr5: 176,387,587-176,390,180 , GRCh38.p12 chr5: 176,960,586-176,963,179 UIMC1
    nsv5393726mobile element deletion1nstd186human GRCh37 chr6: 29,685,488-29,688,079 , GRCh38.p12 chr6: 29,717,711-29,720,302 HCG4P11
    nsv5393431mobile element deletion1nstd186human GRCh37 chr6: 125,708,765-125,711,352 , GRCh38.p12 chr6: 125,387,619-125,390,206 LOC102723341
    nsv5393860mobile element deletion1nstd186human GRCh37 chr6: 56,758,363-56,760,946 , GRCh38.p12 chr6: 56,893,565-56,896,148 DST
    nsv5393850mobile element deletion2nstd186human GRCh37 chr22: 24,195,941-24,198,505 , GRCh38.p12 chr22|NT_187633.1: 90,116-92,680 , GRCh38.p12 chr22: 23,853,754-23,856,318 SLC2A11
    nsv5393799mobile element deletion1nstd186human GRCh37 chr9: 84,324,363-84,326,926 , GRCh38.p12 chr9: 81,709,448-81,712,011 TLE1-DT
    nsv5393554mobile element deletion1nstd186human GRCh37 chr1: 112,835,105-112,837,665 , GRCh38.p12 chr1: 112,292,483-112,295,043 LINC02884
    nsv5393674mobile element deletion2nstd186human GRCh37 chr7: 101,001,266-101,003,795 , GRCh38.p12 chr7: 101,357,985-101,360,514 COL26A1
    nsv5393450mobile element deletion1nstd186human GRCh37 chr10: 12,560,473-12,562,973 , GRCh38.p12 chr10: 12,518,474-12,520,974 CAMK1D
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center