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 324

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142156insertion1nstd232human GRCh37.p13 chr9: 131,226,957-131,226,957 , GRCh38.p12 chr9: 128,464,678-128,464,678 ODF2
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv6876385copy number variation1nstd229human GRCh38 chr9: 128,497,302-128,503,291 , GRCh37.p13 chr9: 131,259,581-131,265,570 GLE1, ODF2
    nsv6866801copy number variation1nstd229human GRCh38 chr9: 128,459,144-128,570,482 , GRCh37.p13 chr9: 131,221,423-131,332,761 RNU7-171P, LOC101929270, 3 more genes
    nsv6864647copy number variation1nstd229human GRCh38 chr9: 128,441,637-128,491,179 , GRCh37.p13 chr9: 131,203,916-131,253,458 LOC100129352, ODF2
    nsv6858409copy number variation1nstd229human GRCh38 chr9: 127,769,112-128,669,700 , GRCh37.p13 chr9: 130,531,391-131,431,979 BBLN, SH2D3C, 47 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6570829inversion1nstd223human GRCh38 chr9: 128,464,215-128,466,056 , GRCh37.p13 chr9: 131,226,494-131,228,335 ODF2
    nsv6568588inversion1nstd223human GRCh38 chr9: 128,464,679-128,465,906 , GRCh37.p13 chr9: 131,226,958-131,228,185 ODF2
    nsv6447200copy number variation1nstd223human GRCh38 chr9: 128,476,252-128,476,846 , GRCh37.p13 chr9: 131,238,531-131,239,125 ODF2
    nsv6438803copy number variation1nstd223human GRCh38 chr9: 126,485,301-128,649,400 , GRCh37.p13 chr9: 129,247,580-131,411,679 MIR199B, FPGS, 72 more genes
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291261copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,523,763-132,604,808 , GRCh38.p12 chr9: 125,761,484-129,842,529 PTPA, AK1, 123 more genes
    nsv6291141copy number variation1nstd102humanUncertain significance GRCh37 chr9: 130,948,822-131,227,396 , GRCh38.p12 chr9: 128,186,543-128,465,117 URM1, TRUB2, 16 more genes
    nsv6282185insertion1nstd214human GRCh38 chr9: 128,463,726-128,463,726 , GRCh37.p13 chr9: 131,226,005-131,226,005 ODF2
    nsv6141548copy number variation1nstd206human GRCh38 chr9: 128,447,966-128,454,597 , GRCh37.p13 chr9: 131,210,245-131,216,876 ODF2
    nsv6137057copy number variation1nstd213human GRCh37 chr9: 130,360,000-135,460,001 , GRCh38.p12 chr9: 127,597,721-132,584,614 CRAT, GLE1, 145 more genes
    nsv6081886insertion1nstd212human GRCh38 chr9: 128,472,132-128,472,132 , GRCh37.p13 chr9: 131,234,411-131,234,411 ODF2
    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