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 299

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098427copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,857,676-135,942,612 , GRCh38.p12 chr9: 129,095,397-133,067,225 ASS1, SETX, 86 more genes
    nsv7098061copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 133,340,833-133,342,151 , GRCh38.p12 chr9: 130,465,446-130,466,764 ASS1
    nsv7098060copy number variation1nstd102humanPathogenic GRCh37 chr9: 133,339,488-133,339,564 , GRCh38.p12 chr9: 130,464,101-130,464,177 ASS1
    nsv7098059copy number variation1nstd102humanPathogenic GRCh37 chr9: 133,319,094-133,377,661 , GRCh38.p12 chr9: 130,443,707-130,502,274 ASS1
    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
    nsv7065209inversion1nstd229human GRCh38 chr9: 130,450,591-130,450,632 , GRCh37.p13 chr9: 133,325,978-133,326,019 ASS1
    nsv7061308inversion1nstd229human GRCh38 chr9: 130,447,009-130,450,554 , GRCh37.p13 chr9: 133,322,396-133,325,941 ASS1
    nsv6877565copy number variation1nstd229human GRCh38 chr9: 130,162,901-130,666,900 , GRCh37.p13 chr9: 133,223,061-133,542,287 MIR6856, LOC107987134, 9 more genes
    nsv6873708copy number variation1nstd229human GRCh38 chr9: 130,471,926-130,474,626 , GRCh37.p13 chr9: 133,347,313-133,350,013 ASS1
    nsv6873267copy number variation1nstd229human GRCh38 chr9: 130,463,768-130,463,817 , GRCh37.p13 chr9: 133,339,155-133,339,204 ASS1
    nsv6873138copy number variation1nstd229human GRCh38 chr9: 130,440,803-130,446,108 , GRCh37.p13 chr9: 133,316,190-133,321,495 ASS1
    nsv6872488copy number variation1nstd229human GRCh38 chr9: 130,421,097-130,581,801 , GRCh37.p13 chr9: 133,296,484-133,457,188 LOC100272217, ASS1, 3 more genes
    nsv6868329copy number variation1nstd229human GRCh38 chr9: 130,446,521-130,446,881 , GRCh37.p13 chr9: 133,321,908-133,322,268 ASS1
    nsv6866968copy number variation1nstd229human GRCh38 chr9: 130,410,059-130,624,963 , GRCh37.p13 chr9: 133,285,446-133,500,350 LOC100272217, ASS1, 4 more genes
    nsv6866212copy number variation1nstd229human GRCh38 chr9: 130,383,401-130,460,400 , GRCh37.p13 chr9: 133,258,788-133,335,787 HMCN2, RN7SL665P, 2 more genes
    nsv6866083copy number variation1nstd229human GRCh38 chr9: 130,296,601-131,144,600 , GRCh37.p13 chr9: 133,223,061-134,019,987 ABL1, PRDM12, 17 more genes
    nsv6865813copy number variation1nstd229human GRCh38 chr9: 130,461,952-130,464,608 , GRCh37.p13 chr9: 133,337,339-133,339,995 ASS1
    nsv6864662copy number variation1nstd229human GRCh38 chr9: 130,213,011-130,477,805 , GRCh37.p13 chr: NaN-NaN NCS1, ASS1, 4 more genes
    nsv6864528copy number variation1nstd229human GRCh38 chr9: 130,478,384-130,483,668 , GRCh37.p13 chr9: 133,353,771-133,359,055 ASS1
    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