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 162

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6990938copy number variation1nstd229human GRCh38 chr17: 76,794,590-76,897,980 , GRCh37.p13 chr17: 74,790,672-74,894,062 LINC02080, MGAT5B, 3 more genes
    nsv6985028copy number variation1nstd229human GRCh38 chr17: 76,853,744-76,857,492 , GRCh37.p13 chr17: 74,849,826-74,853,574 LINC00868
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6982239copy number variation1nstd229human GRCh38 chr17: 76,224,241-77,998,670 , GRCh37.p13 chr17: 74,220,322-75,994,751 MFSD11, PRPSAP1, 59 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6533441copy number variation1nstd223human GRCh38 chr17: 76,853,813-76,854,710 , GRCh37.p13 chr17: 74,849,895-74,850,792 LINC00868
    nsv6530843copy number variation1nstd223human GRCh38 chr17: 76,735,301-77,145,300 , GRCh37.p13 chr17: 74,731,383-75,141,382 SEC14L1, RNU6-97P, 12 more genes
    nsv6520570copy number variation1nstd223human GRCh38 chr17: 76,852,920-76,855,771 , GRCh37.p13 chr17: 74,849,002-74,851,853 LINC00868
    nsv6515853copy number variation1nstd223human GRCh38 chr17: 76,821,329-76,856,023 , GRCh37.p13 chr17: 74,817,411-74,852,105 LINC00868, LOC107985089
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6124300copy number variation1nstd186human GRCh37 chr17: 74,849,907-74,850,829 , GRCh38.p12 chr17: 76,853,825-76,854,747 LINC00868
    nsv5877889copy number variation1nstd209human GRCh38 chr17: 76,853,788-76,854,887 , GRCh37.p13 chr17: 74,849,870-74,850,969 LINC00868
    nsv5532221copy number variation1nstd206human GRCh38 chr17: 76,861,488-76,861,985 , GRCh37.p13 chr17: 74,857,570-74,858,067 LINC00868
    nsv5519568copy number variation1nstd206human GRCh38 chr17: 76,853,825-76,854,747 , GRCh37.p13 chr17: 74,849,907-74,850,829 LINC00868
    nsv5393177copy number variation1nstd186human GRCh37 chr17: 74,849,911-74,850,788 , GRCh38.p12 chr17: 76,853,829-76,854,706 LINC00868
    nsv5390795copy number variation1nstd186human GRCh37 chr17: 74,849,883-74,850,794 , GRCh38.p12 chr17: 76,853,801-76,854,712 LINC00868
    nsv5324390copy number variation1nstd204human GRCh38.p13 chr17: 76,853,796-76,854,739 , GRCh37.p13 chr17: 74,849,878-74,850,821 LINC00868
    nsv5284647copy number variation1nstd204human GRCh38.p13 chr17: 76,853,788-76,854,787 , GRCh37.p13 chr17: 74,849,870-74,850,869 LINC00868
    nsv5016786copy number variation1nstd200human GRCh38 chr17: 76,853,743-76,857,492 , GRCh37.p13 chr17: 74,849,825-74,853,574 LINC00868
    nsv5016785copy number variation1nstd200human GRCh38 chr17: 76,853,800-76,854,712 , GRCh37.p13 chr17: 74,849,882-74,850,794 LINC00868
    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