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 475

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1069251translocation1nstd99human GRCh37 chr9: 140,222,827-140,222,827 , GRCh37 chr9: 140,222,332-140,222,332 , GRCh38.p12 chr9: 137,327,880-137,327,880 , GRCh38.p12 chr9: 137,328,375-137,328,375 EXD3
    nsv1069250translocation1nstd99human GRCh37 chr9: 124,227,820-124,227,820 , GRCh37 chr9: 124,226,912-124,226,912 , GRCh38.p12 chr9: 121,464,634-121,464,634 , GRCh38.p12 chr9: 121,465,542-121,465,542 GGTA1
    nsv1069244translocation1nstd99human GRCh37 chr8: 106,892,022-106,892,022 , GRCh37 chr8: 106,891,553-106,891,553 , GRCh38.p12 chr8: 105,879,325-105,879,325 , GRCh38.p12 chr8: 105,879,794-105,879,794 ZFPM2-AS1
    nsv1069242translocation1nstd99human GRCh37 chr7: 157,162,693-157,162,693 , GRCh37 chr7: 157,162,389-157,162,389 , GRCh38.p12 chr7: 157,369,695-157,369,695 , GRCh38.p12 chr7: 157,369,999-157,369,999 DNAJB6
    nsv1069241translocation1nstd99human GRCh37 chr7: 153,203,642-153,203,642 , GRCh37 chr7: 153,202,939-153,202,939 , GRCh38.p12 chr7: 153,505,854-153,505,854 , GRCh38.p12 chr7: 153,506,557-153,506,557 LOC105375579
    nsv1069235translocation1nstd99human GRCh37 chr6: 158,195,248-158,195,248 , GRCh37 chr6: 158,195,264-158,195,264 , GRCh38.p12 chr6: 157,774,216-157,774,216 , GRCh38.p12 chr6: 157,774,232-157,774,232 SNX9
    nsv1069234translocation1nstd99human GRCh37 chr6: 148,749,493-148,749,493 , GRCh37 chr6: 148,749,557-148,749,557 , GRCh38.p12 chr6: 148,428,357-148,428,357 , GRCh38.p12 chr6: 148,428,421-148,428,421 SASH1
    nsv1069232translocation1nstd99human GRCh37 chr6: 65,022,873-65,022,873 , GRCh37 chr6: 65,023,187-65,023,187 , GRCh38.p12 chr6: 64,312,980-64,312,980 , GRCh38.p12 chr6: 64,313,294-64,313,294 EYS
    nsv1069228translocation1nstd99human GRCh37 chr6: 35,754,574-35,754,574 , GRCh37 chr6: 35,766,761-35,766,761 , GRCh38.p12 chr6: 35,786,797-35,786,797 , GRCh38.p12 chr6: 35,798,984-35,798,984 CLPSL1
    nsv1069225translocation1nstd99human GRCh37 chr6: 1,051,980-1,051,980 , GRCh37 chr6: 1,051,733-1,051,733 , GRCh38.p12 chr6: 1,051,498-1,051,498 , GRCh38.p12 chr6: 1,051,745-1,051,745 LINC01622
    nsv1069224translocation1nstd99human GRCh37 chr5: 79,989,353-79,989,353 , GRCh37 chr5: 79,988,797-79,988,797 , GRCh38.p12 chr5: 80,692,978-80,692,978 , GRCh38.p12 chr5: 80,693,534-80,693,534 MSH3
    nsv1069218translocation1nstd99human GRCh37 chr4: 189,427,846-189,427,846 , GRCh37 chr4: 189,429,664-189,429,664 , GRCh38.p12 chr4: 188,506,692-188,506,692 , GRCh38.p12 chr4: 188,508,510-188,508,510 , GRCh38.p12 chr4|NT_187545.1: 172,095-172,095 LINC01060
    nsv1069213translocation1nstd99human GRCh37 chr4: 100,801,033-100,801,033 , GRCh37 chr4: 100,800,949-100,800,949 , GRCh38.p12 chr4: 99,879,792-99,879,792 , GRCh38.p12 chr4: 99,879,876-99,879,876 LAMTOR3
    nsv1069203translocation1nstd99human GRCh37 chr4: 9,042,818-9,042,818 , GRCh37 chr4: 9,042,787-9,042,787 , GRCh38.p12 chr4: 9,041,061-9,041,061 , GRCh38.p12 chr4: 9,041,092-9,041,092 LOC105369250
    nsv1069198translocation1nstd99human GRCh37 chr3: 15,314,138-15,314,138 , GRCh37 chr3: 15,314,124-15,314,124 , GRCh38.p12 chr3: 15,272,617-15,272,617 , GRCh38.p12 chr3: 15,272,631-15,272,631 SH3BP5
    nsv1069193translocation1nstd99human GRCh37 chr2: 120,417,075-120,417,075 , GRCh37 chr2: 120,418,475-120,418,475 , GRCh38.p12 chr2: 119,659,499-119,659,499 , GRCh38.p12 chr2: 119,660,899-119,660,899 CFAP221
    nsv1069188translocation1nstd99human GRCh37 chr22: 49,001,262-49,001,262 , GRCh37 chr22: 49,001,029-49,001,029 , GRCh38.p12 chr22: 48,605,217-48,605,217 , GRCh38.p12 chr22: 48,605,450-48,605,450 TAFA5
    nsv1069186translocation1nstd99human GRCh37 chr21: 46,474,902-46,474,902 , GRCh37 chr21: 46,475,028-46,475,028 , GRCh38.p12 chr21: 45,054,987-45,054,987 , GRCh38.p12 chr21: 45,055,113-45,055,113 LOC105372836
    nsv1069184translocation1nstd99human GRCh37 chr20: 62,197,895-62,197,895 , GRCh37 chr20: 62,197,869-62,197,869 , GRCh38.p12 chr20: 63,566,516-63,566,516 , GRCh38.p12 chr20: 63,566,542-63,566,542 HELZ2
    nsv1069182translocation1nstd99human GRCh37 chr20: 23,295,311-23,295,311 , GRCh37 chr20: 23,295,293-23,295,293 , GRCh38.p12 chr20: 23,314,656-23,314,656 , GRCh38.p12 chr20: 23,314,674-23,314,674 NXT1-AS1
    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