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 96

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5533679copy number variation1nstd206human GRCh38 chr17: 28,318,716-28,321,753 , GRCh37.p13 chr17|NW_003871090.1: 584-3,621 , GRCh37.p13 chr17: 26,645,742-26,648,779 TMEM97
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675321copy number variation1nstd102humanPathogenic GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689 ABHD15, LOC100420408, 112 more genes
    nsv4507024mobile element insertion1nstd166human GRCh37.p13 chr17: 26,647,348-26,647,348 , GRCh38.p12 chr17: 28,320,322-28,320,322 TMEM97
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4379025copy number variation1nstd173human GRCh37 chr17: 25,307,567-27,710,963 , GRCh38.p12 chr17: 26,980,541-29,383,945 , MIR451A, 91 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4243070copy number variation1nstd166human GRCh37.p13 chr17: 26,517,014-26,775,312 , GRCh38.p12 chr17: 28,189,988-28,448,294 IFT20, H3P41, 17 more genes
    nsv4242342copy number variation1nstd166human GRCh37.p13 chr17: 26,653,988-26,654,123 , GRCh38.p12 chr17: 28,326,962-28,327,097 IFT20, TMEM97
    nsv4233979copy number variation1nstd166human GRCh37.p13 chr17: 26,644,070-26,644,681 , GRCh38.p12 chr17: 28,317,044-28,317,655 TMEM97
    nsv3972367copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 25,403,446-31,685,464 , GRCh38.p12 chr17: 27,076,420-33,358,446 ASIC2, AK4P1, 190 more genes
    nsv3962910copy number variation1nstd168human GRCh38 chr17: 28,276,708-28,319,917 , GRCh37.p13 chr17: 26,603,734-26,645,158 TMEM97, KRT18P55
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3909986copy number variation1nstd102humanBenign GRCh38 chr17: 28,283,125-28,904,397 , GRCh37 chr17: 26,610,151-27,231,415 , NCBI36 chr17: 23,634,278-24,255,541 SLC13A2, MIR144, 44 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3903658copy number variation1nstd102humandrug response GRCh37 chr17: 25,248,166-30,645,676 , GRCh38.p12 chr17: 26,935,981-32,318,657 KRT18P55, CPDP1, 179 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
    nsv3898099copy number variation1nstd102humanUncertain significance GRCh37 chr17: 21,308,559-26,655,801 , GRCh38.p12 chr17: 21,405,247-28,328,775 MTND4LP8, MIR4522, 71 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