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 116

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070638inversion1nstd229human GRCh38 chr17: 20,843,363-22,437,673 , GRCh37.p13 chr17: 20,746,676-21,937,002 LOC107987246, PDLIM1P2, 33 more genes
    nsv7061315inversion1nstd229human GRCh38 chr17: 21,247,652-21,253,558 , GRCh37.p13 chr17: 21,150,965-21,156,870 NATD1
    nsv6996359copy number variation1nstd229human GRCh38 chr17: 21,240,218-21,240,263 , GRCh37.p13 chr17: 21,143,531-21,143,576 NATD1
    nsv6985185copy number variation1nstd229human GRCh38 chr17: 21,238,780-21,240,831 , GRCh37.p13 chr17: 21,142,093-21,144,144 NATD1
    nsv6511683copy number variation1nstd223human GRCh38 chr17: 21,238,775-21,240,825 , GRCh37.p13 chr17: 21,142,088-21,144,138 NATD1
    nsv6502353copy number variation1nstd223human GRCh38 chr17: 21,111,202-21,303,044 , GRCh37.p13 chr17: 21,014,515-21,206,356 EIF1P5, MAP2K3, 5 more genes
    nsv6315238complex substitution1nstd102humanPathogenic GRCh37 chr17: 14,876,984-22,124,952 , GRCh38.p12 chr17: 14,973,667-22,625,625 ADORA2B, ALDH3A1, 281 more genes
    nsv5930574copy number variation1nstd209human GRCh38 chr17: 21,252,976-21,253,058 , GRCh37.p13 chr17: 21,156,289-21,156,371 NATD1
    nsv5868230copy number variation2nstd209human GRCh38 chr17: 21,252,605-21,253,641 , GRCh37.p13 chr17: 21,155,918-21,156,953 NATD1
    nsv5670902inversion1nstd207human GRCh37.p13 chr17: 19,143,942-21,250,947 , GRCh38 chr17: 19,240,629-21,558,840 , ALDH3A1, 86 more genes
    nsv5159749mobile element insertion1nstd203human GRCh38 chr17: 21,251,869-21,251,883 , GRCh37.p13 chr17: 21,155,182-21,155,196 NATD1
    nsv5023763copy number variation1nstd200human GRCh38 chr17: 21,119,430-21,252,254 , GRCh37.p13 chr17: 21,022,743-21,155,567 DHRS7B, TMEM11-DT, 3 more genes
    nsv5023762copy number variation1nstd200human GRCh38 chr17: 21,111,202-21,303,046 , GRCh37.p13 chr17: 21,014,515-21,206,358 TMEM11, EIF1P5, 5 more genes
    nsv5010016copy number variation1nstd200human GRCh38 chr17: 21,253,885-21,255,070 , GRCh37.p13 chr17: 21,157,197-21,158,382 NATD1
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4629444copy number variation1nstd183human GRCh37 chr17: 21,156,503-21,156,548 , GRCh38.p12 chr17: 21,253,190-21,253,236 NATD1
    nsv4510677mobile element insertion1nstd166human GRCh37.p13 chr17: 21,155,182-21,155,182 , GRCh38.p12 chr17: 21,251,869-21,251,869 NATD1
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3922944copy number variation1nstd102humanUncertain significance NCBI36 chr17: 19,587,938-21,442,522 , GRCh37 chr17: 19,647,346-21,501,929 , GRCh38 chr17: 19,744,033-21,598,663 RNU6-258P, CCDC144NL, 61 more genes
    nsv3922250copy number variation1nstd102humanUncertain significance GRCh38 chr17: 20,935,766-21,621,469 , GRCh37 chr17: 20,839,079-21,529,632 , NCBI36 chr17: 20,779,671-21,471,956 LOC101930665, TMEM11-DT, 15 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