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 89

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5381009copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,856,492-37,884,297 , GRCh38.p12 chr17: 39,700,239-39,728,044 MIEN1, ERBB2, 1 more genes
    nsv4625569copy number variation1nstd183human GRCh37 chr17: 37,736,785-37,904,211 , GRCh38.p12 chr17: 39,580,532-39,747,958 ERBB2, PGAP3, 9 more genes
    nsv4621031copy number variation1nstd183human GRCh37 chr17: 37,885,447-37,885,501 , GRCh38.p12 chr17: 39,729,194-39,729,248 MIEN1
    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
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    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
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 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
    nsv3903293copy number variation1nstd102humanUncertain significance GRCh37 chr17: 36,972,794-38,033,708 , GRCh38.p12 chr17: 38,816,541-39,877,455 LASP1NB, MED1, 46 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
    nsv3166061copy number variation1nstd151human GRCh37 chr17: 37,880,162-37,947,841 , GRCh38.p12 chr17: 39,723,909-39,791,588 ERBB2, GRB7, 3 more genes
    nsv3165473copy number variation1nstd151human GRCh37 chr17: 37,809,782-37,949,191 , GRCh38.p12 chr17: 39,653,529-39,792,938 MIR4728, TCAP, 7 more genes
    nsv3164376copy number variation1nstd151human GRCh37 chr17: 37,786,194-38,080,461 , GRCh38.p12 chr17: 39,629,941-39,924,208 MIR4728, RPL39P4, 13 more genes
    nsv3163848copy number variation1nstd151human GRCh37 chr17: 37,371,041-38,130,086 , GRCh38.p12 chr17: 39,214,788-39,973,833 , STAC2, 26 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