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 225

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094979copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr17: 48,068,881-48,278,874 , GRCh38.p12 chr17: 49,991,517-50,201,513 PICART1, H1-9P, 8 more genes
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6526697copy number variation1nstd223human GRCh38 chr17: 50,082,397-50,088,881 , GRCh37.p13 chr17: 48,159,761-48,166,245 ITGA3
    nsv6522605copy number variation1nstd223human GRCh38 chr17: 50,085,527-50,086,307 , GRCh37.p13 chr17: 48,162,891-48,163,671 ITGA3
    nsv6519749copy number variation1nstd223human GRCh38 chr17: 50,071,790-50,073,647 , GRCh37.p13 chr17: 48,149,154-48,151,011 ITGA3
    nsv6199252copy number variation1nstd214human GRCh38 chr17: 50,085,677-50,085,740 , GRCh37.p13 chr17: 48,163,041-48,163,104 ITGA3
    nsv6195842copy number variation1nstd214human GRCh38 chr17: 50,085,805-50,085,858 , GRCh37.p13 chr17: 48,163,169-48,163,222 ITGA3
    nsv6189902copy number variation1nstd214human GRCh38 chr17: 50,085,726-50,085,789 , GRCh37.p13 chr17: 48,163,090-48,163,153 ITGA3
    nsv6131390insertion1nstd186human GRCh37 chr17: 48,140,446-48,140,448 , GRCh38.p12 chr17: 50,063,082-50,063,084 ITGA3
    nsv6099442insertion1nstd212human GRCh38 chr17: 50,086,098-50,086,098 , GRCh37.p13 chr17: 48,163,462-48,163,462 ITGA3
    nsv6097529insertion1nstd212human GRCh38 chr17: 50,085,908-50,085,908 , GRCh37.p13 chr17: 48,163,272-48,163,272 ITGA3
    nsv6088810insertion1nstd212human GRCh38 chr17: 50,083,748-50,083,748 , GRCh37.p13 chr17: 48,161,112-48,161,112 ITGA3
    nsv6087540insertion1nstd212human GRCh38 chr17: 50,085,759-50,085,759 , GRCh37.p13 chr17: 48,163,123-48,163,123 ITGA3
    nsv6085168insertion1nstd212human GRCh38 chr17: 50,085,934-50,085,934 , GRCh37.p13 chr17: 48,163,298-48,163,298 ITGA3
    nsv6084448insertion1nstd212human GRCh38 chr17: 50,085,803-50,085,803 , GRCh37.p13 chr17: 48,163,167-48,163,167 ITGA3
    nsv6081018insertion1nstd212human GRCh38 chr17: 50,086,036-50,086,036 , GRCh37.p13 chr17: 48,163,400-48,163,400 ITGA3
    nsv6035794copy number variation1nstd212human GRCh38 chr17: 50,085,672-50,086,196 , GRCh37.p13 chr17: 48,163,036-48,163,560 ITGA3
    nsv6032540copy number variation1nstd212human GRCh38 chr17: 50,085,802-50,085,866 , GRCh37.p13 chr17: 48,163,166-48,163,230 ITGA3
    nsv6022869copy number variation1nstd212human GRCh38 chr17: 50,085,846-50,085,913 , GRCh37.p13 chr17: 48,163,210-48,163,277 ITGA3
    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