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 248

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141116copy number variation1nstd232human GRCh37.p13 chr17: 80,674,389-80,674,468 , GRCh38.p12 chr17: 82,716,513-82,716,592 FN3KRP, LOC101929552
    nsv7137148copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,656,331-81,009,672 , GRCh38.p12 chr17: 82,698,455-83,051,796 ZNF750, FN3KRP, 5 more genes
    nsv7098933copy number variation1nstd102humanUncertain significance GRCh38 chr17: 82,004,063-83,087,346 , GRCh37.p13 chr17: 79,961,939-81,045,222 ZNF750, LINC01970, 37 more genes
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095424copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,332,201-80,758,892 , GRCh38.p12 chr17: 82,374,325-82,801,016 CYBC1, TRX-CAT1-8, 15 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7067498inversion1nstd229human GRCh38 chr17: 82,700,440-82,715,184 , GRCh37.p13 chr17: 80,658,316-80,673,060 FN3KRP, LOC101929552
    nsv7063392inversion1nstd229human GRCh38 chr17: 82,609,707-82,780,313 , GRCh37.p13 chr17: 80,567,583-80,738,189 RAB40B, FN3KRP, 5 more genes
    nsv6995894copy number variation1nstd229human GRCh38 chr17: 82,528,831-82,827,183 , GRCh37.p13 chr17: 80,486,707-80,785,059 LOC105371942, FN3KRP, 8 more genes
    nsv6995527copy number variation1nstd229human GRCh38 chr17: 82,681,594-82,916,948 , GRCh37.p13 chr17: 80,639,470-80,874,824 LOC101929552, TBCD, 4 more genes
    nsv6991955copy number variation1nstd229human GRCh38 chr17: 82,718,702-82,725,757 , GRCh37.p13 chr17: 80,676,578-80,683,633 FN3KRP
    nsv6990525copy number variation1nstd229human GRCh38 chr17: 82,708,698-82,716,353 , GRCh37.p13 chr17: 80,666,574-80,674,229 FN3KRP, LOC101929552
    nsv6985899copy number variation1nstd229human GRCh38 chr17: 82,709,064-82,956,275 , GRCh37.p13 chr17: 80,666,940-80,914,151 FN3K, TBCD, 4 more genes
    nsv6985281copy number variation1nstd229human GRCh38 chr17: 82,654,201-82,957,097 , GRCh37.p13 chr17: 80,612,077-80,914,973 B3GNTL1, MIR4525, 6 more genes
    nsv6983693copy number variation1nstd229human GRCh38 chr17: 82,697,149-82,736,865 , GRCh37.p13 chr17: 80,655,025-80,694,741 RAB40B, FN3K, 2 more genes
    nsv6637647copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,585,033-81,041,938 , GRCh38.p12 chr17: 82,627,157-83,084,062 ZNF750, FN3KRP, 8 more genes
    nsv6634437copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 80,496,771-81,195,210 , GRCh38.p12 chr17: 82,538,895-83,247,441 FOXK2, TBCD, 16 more genes
    nsv6532503copy number variation1nstd223human GRCh38 chr17: 82,709,064-82,956,275 , GRCh37.p13 chr17: 80,666,940-80,914,151 FN3KRP, B3GNTL1, 4 more genes
    nsv6529829copy number variation1nstd223human GRCh38 chr17: 82,664,860-83,182,172 , GRCh37.p13 chr17: 80,622,736-81,129,941 LOC101929552, TBCD, 9 more genes
    nsv6525583copy number variation1nstd223human GRCh38 chr17: 82,717,967-82,718,221 , GRCh37.p13 chr17: 80,675,843-80,676,097 FN3KRP
    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