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 740

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148137copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,805,785-32,686,484 , GRCh38.p12 chr15: 30,513,582-32,394,283 LINC02352, CHRNA7, 37 more genes
    nsv7148111copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,742,396-28,567,325 , GRCh38.p12 chr15: 23,319,714-28,322,179 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD116-18, PWAR4, 246 more genes
    nsv7148103copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,850,097-32,693,726 , GRCh38.p12 chr15: 30,557,894-32,401,525 LOC400347, GOLGA8Q, 37 more genes
    nsv7148096copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,854,238-32,892,694 , GRCh38.p12 chr15: 30,562,035-32,600,493 MTMR10, GOLGA8Q, 50 more genes
    nsv7137213copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-30,386,398 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-30,094,195 TVP23BP1, SNORD115-1, 247 more genes
    nsv7098888copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,888,853-32,539,607 , GRCh38.p12 chr15: 30,596,650-32,247,406 FAN1, ARHGAP11B, 26 more genes
    nsv7098883copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,406,271-28,566,579 , GRCh38.p12 chr15: 23,319,714-28,321,433 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC105370739, SNORD116-27, 246 more genes
    nsv7093407copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-28,544,662 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,299,516 UBE2CP4, SERPINE4P, 246 more genes
    nsv7070433inversion1nstd229human GRCh38 chr15: 28,680,335-30,817,180 , GRCh37.p13 chr15: 28,925,481-31,109,383 RNU6-17P, RN7SL628P, 54 more genes
    nsv7068342inversion1nstd229human GRCh38 chr15: 29,120,877-31,530,094 , GRCh37.p13 chr15: 29,413,080-31,822,297 ULK4P2, TRPM1, 57 more genes
    nsv7065318inversion1nstd229human GRCh38 chr15: 29,942,582-32,138,315 , GRCh37.p13 chr15: 30,234,785-32,430,516 GOLGA8T, ARHGAP11B, 52 more genes
    nsv7061220inversion1nstd229human GRCh38 chr15: 28,848,197-32,920,244 , GRCh37.p13 chr15: 29,093,343-33,212,445 LOC105376704, WHAMMP1, 96 more genes
    nsv6959394copy number variation1nstd229human GRCh38 chr15: 30,097,501-30,596,100 , GRCh37.p13 chr15: 30,389,704-30,888,303 WHAMMP4, GOLGA8T, 22 more genes
    nsv6637778copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,601 , GRCh38.p12 chr15: 23,319,714-28,300,455 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC107984779, ULK4P1, 246 more genes
    nsv6637596copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,290,787-28,560,269 , GRCh38.p12 chr15: 23,319,714-28,315,123 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD115-23, DEPDC1P1, 246 more genes
    nsv6637553copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-30,386,553 , GRCh38.p12 chr15: 23,319,714-30,094,350 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 FAN1, LOC105370751, 247 more genes
    nsv6637528copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,370,018-32,446,830 , GRCh38.p12 chr15: 30,077,815-32,154,629 OTUD7A, LOC105370752, 49 more genes
    nsv6637399copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,355 , GRCh38.p12 chr15: 23,319,714-28,300,209 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 DNM1P28, MIR4508, 246 more genes
    nsv6637197copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,540,415-32,446,830 , GRCh38.p12 chr15: 28,295,269-32,154,629 RN7SL238P, DEPDC1P1, 90 more genes
    nsv6635440copy number variation1nstd227human GRCh37 chr15: 30,657,952-31,010,475 , GRCh38.p12 chr15: 30,365,749-30,718,272 CHRFAM7A, ARHGAP11B, 17 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