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 148

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096216copy number variation2nstd102humanUncertain significance GRCh37 chr2: 178,095,513-179,914,668 , GRCh38.p12 chr2: 177,230,785-179,049,941 CYCTP, LOC100130691, 29 more genes
    nsv7057414inversion1nstd229human GRCh38 chr2: 178,126,133-178,126,198 , GRCh37.p13 chr2: 178,990,860-178,990,925 RBM45
    nsv6696639copy number variation1nstd229human GRCh38 chr2: 178,117,899-178,117,927 , GRCh37.p13 chr2: 178,982,626-178,982,654 RBM45
    nsv6690866copy number variation1nstd229human GRCh38 chr2: 178,126,998-178,128,105 , GRCh37.p13 chr2: 178,991,725-178,992,832 RBM45
    nsv6685015copy number variation1nstd229human GRCh38 chr2: 178,110,189-178,114,122 , GRCh37.p13 chr2: 178,974,916-178,978,849 RBM45
    nsv6637115copy number variation1nstd102humanPathogenic GRCh37 chr2: 175,143,352-180,999,636 , GRCh38.p12 chr2: 174,278,624-180,134,909 RNU6-5P, LOC101927073, 107 more genes
    nsv6548314inversion1nstd223human GRCh38 chr2: 177,986,552-178,841,553 , GRCh37.p13 chr2: 178,851,279-179,706,280 RNU6-629P, RNU5E-9P, 17 more genes
    nsv6343414copy number variation1nstd223human GRCh38 chr2: 178,122,125-178,122,606 , GRCh37.p13 chr2: 178,986,852-178,987,333 RBM45
    nsv6340136copy number variation1nstd223human GRCh38 chr2: 178,107,201-178,115,300 , GRCh37.p13 chr2: 178,971,928-178,980,027 PDE11A, RBM45
    nsv6337282copy number variation1nstd223human GRCh38 chr2: 178,125,529-178,126,348 , GRCh37.p13 chr2: 178,990,256-178,991,075 RBM45
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6134634copy number variation1nstd213human GRCh37 chr2: 178,870,000-179,940,001 , GRCh38.p12 chr2: 178,005,273-179,075,274 TTN, PRKRA, 18 more genes
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 more genes
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5381341copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,999,572-182,774,361 , GRCh38.p12 chr2: 171,143,062-181,909,634 ALDH7A1P2, LOC101927055, 174 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 RBM45, LOC102724194, 258 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728615copy number variation1nstd102humanUncertain significance GRCh37 chr2: 177,542,722-179,538,238 , GRCh38.p12 chr2: 176,677,994-178,673,511 MIR3128, PLEKHA3, 40 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