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 268

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7073296inversion1nstd229human GRCh38 chr9: 129,033,186-129,036,921 , GRCh37.p13 chr9: 131,795,465-131,799,200 MIGA2
    nsv7070239inversion1nstd229human GRCh38 chr9: 128,869,438-129,153,886 , GRCh37.p13 chr9: 131,631,717-131,916,165 DOLK, PTPA, 10 more genes
    nsv6877343copy number variation1nstd229human GRCh38 chr9: 129,070,854-129,075,199 , GRCh37.p13 chr9: 131,833,133-131,837,478 MIGA2
    nsv6866061copy number variation1nstd229human GRCh38 chr9: 129,066,317-129,072,785 , GRCh37.p13 chr9: 131,828,596-131,835,064 MIGA2
    nsv6860303copy number variation1nstd229human GRCh38 chr9: 129,063,380-129,063,439 , GRCh37.p13 chr9: 131,825,659-131,825,718 MIGA2
    nsv6573724inversion1nstd223human GRCh38 chr9: 129,065,086-129,066,659 , GRCh37.p13 chr9: 131,827,365-131,828,938 MIGA2
    nsv6567032inversion1nstd223human GRCh38 chr9: 129,057,867-129,058,124 , GRCh37.p13 chr9: 131,820,146-131,820,403 MIGA2
    nsv6441426copy number variation1nstd223human GRCh38 chr9: 129,043,740-129,044,142 , GRCh37.p13 chr9: 131,806,019-131,806,421 MIGA2
    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
    nsv6175274copy number variation1nstd214human GRCh38 chr9: 129,063,380-129,063,438 , GRCh37.p13 chr9: 131,825,659-131,825,717 MIGA2
    nsv6142156copy number variation1nstd206human GRCh38 chr9: 129,036,552-129,154,552 , GRCh37.p13 chr9: 131,798,831-131,916,831 CRAT, DOLPP1, 2 more genes
    nsv6141444copy number variation1nstd206human GRCh38 chr9: 129,058,546-129,072,779 , GRCh37.p13 chr9: 131,820,825-131,835,058 MIGA2
    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
    nsv6012716copy number variation1nstd212human GRCh38 chr9: 129,066,818-129,066,992 , GRCh37.p13 chr9: 131,829,097-131,829,271 MIGA2
    nsv6009473copy number variation1nstd212human GRCh38 chr9: 129,052,303-129,053,534 , GRCh37.p13 chr9: 131,814,582-131,815,813 MIGA2
    nsv5920228copy number variation1nstd209human GRCh38 chr9: 129,043,791-129,044,083 , GRCh37.p13 chr9: 131,806,070-131,806,362 MIGA2
    nsv5914121copy number variation1nstd209human GRCh38 chr9: 129,063,380-129,063,438 , GRCh37.p13 chr9: 131,825,659-131,825,717 MIGA2
    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