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 657

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077141inversion1nstd229human GRCh38 chr12: 104,535,921-104,539,998 , GRCh37.p13 chr12: 104,929,699-104,933,776 CHST11
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7070458inversion1nstd229human GRCh38 chr12: 104,753,206-104,753,325 , GRCh37.p13 chr12: 105,146,984-105,147,103 CHST11
    nsv7069613inversion1nstd229human GRCh38 chr12: 104,413,888-104,490,465 , GRCh37.p13 chr12: 104,807,666-104,884,243 LOC105369949, CHST11
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv7066553inversion1nstd229human GRCh38 chr12: 104,402,174-104,477,601 , GRCh37.p13 chr12: 104,795,952-104,871,379 CHST11, LOC105369949
    nsv7063353inversion1nstd229human GRCh38 chr12: 104,713,600-104,713,668 , GRCh37.p13 chr12: 105,107,378-105,107,446 CHST11
    nsv7059081inversion1nstd229human GRCh38 chr12: 104,461,602-104,461,718 , GRCh37.p13 chr12: 104,855,380-104,855,496 CHST11
    nsv6937645copy number variation1nstd229human GRCh38 chr12: 104,702,488-104,705,262 , GRCh37.p13 chr12: 105,096,266-105,099,040 CHST11
    nsv6937009copy number variation1nstd229human GRCh38 chr12: 104,721,380-104,730,272 , GRCh37.p13 chr12: 105,115,158-105,124,050 CHST11
    nsv6936229copy number variation1nstd229human GRCh38 chr12: 104,591,466-104,598,011 , GRCh37.p13 chr12: 104,985,244-104,991,789 MIR3922, CHST11
    nsv6936099copy number variation1nstd229human GRCh38 chr12: 104,626,921-104,632,440 , GRCh37.p13 chr12: 105,020,699-105,026,218 CHST11
    nsv6936062copy number variation1nstd229human GRCh38 chr12: 104,466,158-104,530,959 , GRCh37.p13 chr12: 104,859,936-104,924,737 CHST11
    nsv6935007copy number variation1nstd229human GRCh38 chr12: 104,561,517-104,587,240 , GRCh37.p13 chr12: 104,955,295-104,981,018 CHST11
    nsv6934739copy number variation1nstd229human GRCh38 chr12: 104,744,288-104,752,502 , GRCh37.p13 chr12: 105,138,066-105,146,280 CHST11
    nsv6934424copy number variation1nstd229human GRCh38 chr12: 104,695,464-104,695,495 , GRCh37.p13 chr12: 105,089,242-105,089,273 CHST11
    nsv6933625copy number variation1nstd229human GRCh38 chr12: 104,720,171-104,722,475 , GRCh37.p13 chr12: 105,113,949-105,116,253 CHST11
    nsv6933534copy number variation1nstd229human GRCh38 chr12: 104,484,217-104,492,799 , GRCh37.p13 chr12: 104,877,995-104,886,577 CHST11
    nsv6932595copy number variation1nstd229human GRCh38 chr12: 104,477,501-104,490,500 , GRCh37.p13 chr12: 104,871,279-104,884,278 CHST11
    nsv6931071copy number variation1nstd229human GRCh38 chr12: 104,493,538-104,496,541 , GRCh37.p13 chr12: 104,887,316-104,890,319 CHST11
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

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