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 113

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070278inversion1nstd229human GRCh38 chr9: 85,364,427-88,288,635 , GRCh37.p13 chr9: 87,979,342-90,903,550 LOC105376121, CTSL3P, 57 more genes
    nsv7068881inversion1nstd229human GRCh38 chr9: 85,364,378-88,276,332 , GRCh37.p13 chr9: 87,979,293-90,891,247 LOC100129202, LOC100287212, 57 more genes
    nsv7067775inversion1nstd229human GRCh38 chr9: 83,864,984-85,758,960 , GRCh37.p13 chr9: 86,479,899-88,373,875 LOC105376335, LOC101927575, 20 more genes
    nsv7065594inversion1nstd229human GRCh38 chr9: 85,426,274-86,082,250 , GRCh37.p13 chr9: 88,041,189-88,697,165 PHB1P7, LOC105376121, 8 more genes
    nsv7059796inversion1nstd229human GRCh38 chr9: 83,885,955-85,843,950 , GRCh37.p13 chr9: 86,500,870-88,458,865 HNRNPK, LOC105376121, 21 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
    nsv6568042inversion1nstd223human GRCh38 chr9: 77,399,209-87,276,767 , GRCh37.p13 chr9: 80,014,125-89,891,682 , LOC105376119, 118 more genes
    nsv6556699inversion1nstd223human GRCh38 chr9: 83,902,711-85,826,507 , GRCh37.p13 chr9: 86,517,626-88,441,422 KIF27, RMI1, 21 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314204copy number variation1nstd102humanUncertain significance GRCh37 chr9: 87,881,345-88,749,247 , GRCh38.p12 chr9: 85,266,430-86,134,332 AGTPBP1, LOC105376121, 12 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 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
    nsv6290004inversion1nstd102humanLikely pathogenic GRCh38.p12 chr9: 12,246,100-98,797,096 , GRCh37 chr9: 12,246,100-101,559,378 ACO1, PLIN2, 1215 more genes
    nsv6108125inversion1nstd212human GRCh38 chr9: 83,888,038-85,852,545 , GRCh37.p13 chr9: 86,502,953-88,467,460 , HNRNPK, 22 more genes
    nsv5036269inversion1nstd200human GRCh38 chr9: 79,108,237-87,224,469 , GRCh37.p13 chr9: 81,723,153-89,839,384 , RMI1, 100 more genes
    nsv4767221inversion1nstd199human GRCh37 chr9: 86,502,949-88,456,795 , GRCh38.p12 chr9: 83,888,034-85,841,880 , HNRNPK, 22 more genes
    nsv4608006copy number variation1nstd183human GRCh37 chr9: 87,419,506-88,217,970 , GRCh38.p12 chr9: 84,804,591-85,603,055 LOC105376121, LOC105376118, 8 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455864copy number variation1nstd102humanUncertain significance GRCh37 chr9: 86,434,567-88,413,614 , GRCh38.p12 chr9: 83,819,652-85,798,699 HNRNPK, LOC105376121, 21 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    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