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 141

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889414copy number variation1nstd209human GRCh38 chr5: 122,061,092-122,061,452 , GRCh37.p13 chr5: 121,396,787-121,397,147 LOX, SRFBP1
    nsv5458709copy number variation1nstd206human GRCh38 chr5: 122,061,092-122,061,469 , GRCh37.p13 chr5: 121,396,787-121,397,164 LOX, SRFBP1
    nsv5455701copy number variation1nstd206human GRCh38 chr5: 122,062,407-122,062,541 , GRCh37.p13 chr5: 121,398,102-121,398,236 SRFBP1, LOX
    nsv5377995translocation1nstd200human GRCh38 chr5: 122,061,469-122,061,469 , GRCh38 chr5: 122,061,091-122,061,091 , GRCh37.p13 chr5: 121,397,164-121,397,164 , GRCh37.p13 chr5: 121,396,786-121,396,786 SRFBP1, LOX
    nsv5340080translocation1nstd200human GRCh37 chr5: 121,397,164-121,397,164 , GRCh37 chr5: 121,396,787-121,396,787 , GRCh38.p12 chr5: 122,061,092-122,061,092 , GRCh38.p12 chr5: 122,061,469-122,061,469 SRFBP1, LOX
    nsv5326086translocation1nstd204human GRCh37.p13 chr5: 121,396,786-121,396,786 , GRCh37.p13 chr5: 121,397,164-121,397,164 , GRCh38.p13 chr5: 122,061,091-122,061,091 , GRCh38.p13 chr5: 122,061,469-122,061,469 LOX, SRFBP1
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4737550copy number variation1nstd199human GRCh37 chr5: 121,396,782-121,397,145 , GRCh38.p12 chr5: 122,061,087-122,061,450 LOX, SRFBP1
    nsv4597705copy number variation1nstd183human GRCh37 chr5: 121,398,910-121,402,492 , GRCh38.p12 chr5: 122,063,215-122,066,797 SRFBP1, LOX
    nsv4522111copy number variation1nstd166human GRCh37.p13 chr5: 121,396,787-121,397,164 , GRCh38.p12 chr5: 122,061,092-122,061,469 LOX, SRFBP1
    nsv4455983copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762 LOC345576, LOC107986436, 419 more genes
    nsv4455632copy number variation1nstd102humanUncertain significance GRCh37 chr5: 120,785,278-122,419,820 , GRCh38.p12 chr5: 121,449,583-123,084,125 FTMT, LOX, 25 more genes
    nsv4455582copy number variation1nstd102humanUncertain significance GRCh37 chr5: 120,035,723-121,808,658 , GRCh38.p12 chr5: 120,700,028-122,472,963 LOC105379150, RPL23AP44, 18 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4345524sequence alteration1nstd166human GRCh37.p13 chr5: 120,941,265-127,230,417 , GRCh38.p12 chr5: 121,605,570-127,894,725 LOX, PPIC, 78 more genes
    nsv4321173inversion1nstd166human GRCh37.p13 chr5: 86,365,040-130,339,409 , GRCh38.p12 chr5: 87,069,223-131,003,716 , APC, 481 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