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 157

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7098689copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,801,983-4,802,032 , GRCh38 chr17: 4,898,688-4,898,737 CHRNE, C17orf107
    nsv7093604insertion1nstd102humanPathogenic GRCh37 chr17: 4,802,827-4,802,827 , GRCh38 chr17: 4,899,532-4,899,532 CHRNE, C17orf107
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv7068795inversion1nstd229human GRCh38 chr17: 4,882,859-5,367,549 , GRCh37.p13 chr17: 4,786,154-5,270,844 CAMTA2, LOC105371505, 27 more genes
    nsv6991124copy number variation1nstd229human GRCh38 chr17: 4,897,777-4,900,911 , GRCh37.p13 chr17: 4,801,072-4,804,206 C17orf107, MINK1, 1 more genes
    nsv6985628copy number variation1nstd229human GRCh38 chr17: 4,867,448-4,906,651 , GRCh37.p13 chr17: 4,770,743-4,809,946 CHRNE, MINK1, 2 more genes
    nsv6982770copy number variation1nstd229human GRCh38 chr17: 3,468,201-5,384,400 , GRCh37.p13 chr17: 3,371,495-5,287,720 SLC25A11, CAMKK1, 83 more genes
    nsv6982450copy number variation1nstd229human GRCh38 chr17: 1,838,614-7,660,509 , GRCh37.p13 chr17: 1,741,908-7,563,827 NCBP3, OR1P1, 242 more genes
    nsv6638055copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,658,216-5,266,343 , GRCh38.p12 chr17: 4,754,921-5,363,048 RABEP1, SLC25A11, 33 more genes
    nsv6592364inversion1nstd223human GRCh38 chr17: 2,078,667-6,081,513 , GRCh37.p13 chr17: 1,981,961-5,984,833 MYBBP1A, CXCL16, 143 more genes
    nsv6589878inversion1nstd223human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 ASGR1, KIF1C-AS1, 321 more genes
    nsv6502799copy number variation1nstd223human GRCh38 chr17: 4,901,974-4,902,776 , GRCh37.p13 chr17: 4,805,269-4,806,071 CHRNE, C17orf107
    nsv6502092copy number variation1nstd223human GRCh38 chr17: 4,869,520-4,948,195 , GRCh37.p13 chr17: 4,772,815-4,851,490 MINK1, C17orf107, 7 more genes
    nsv6314802copy number variation1nstd102humanUncertain significance GRCh38 chr17: 4,772,213-5,119,909 , GRCh37.p13 chr17: 4,675,508-5,023,204 PFN1, ZNF232, 28 more genes
    nsv6314134copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,113,551-5,023,913 , GRCh38.p12 chr17: 4,210,256-5,120,618 ZNF232-AS1, RN7SL774P, 52 more genes
    nsv6310179copy number variation1nstd102humanPathogenic GRCh37 chr17: 4,805,539-4,806,690 , GRCh38.p12 chr17: 4,902,244-4,903,395 C17orf107, CHRNE
    nsv6310178copy number variation1nstd102humanPathogenic GRCh37 chr17: 4,802,021-4,802,196 , GRCh38.p12 chr17: 4,898,726-4,898,901 CHRNE, C17orf107
    nsv6133245copy number variation1nstd213human GRCh37 chr17: 4,010,000-8,220,001 , GRCh38.p12 chr17: 4,106,706-8,316,683 ACADVL, ALOX12, 220 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