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 128

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093820copy number variation1nstd102humanUncertain significance GRCh37 chr11: 101,374,735-103,349,981 , GRCh38.p12 chr11: 101,504,004-103,479,253 WTAPP1, TMEM123, 40 more genes
    nsv7068895inversion1nstd229human GRCh38 chr11: 100,518,680-109,308,656 , GRCh37.p13 chr11: 100,389,411-109,179,383 LINC02719, RNA5SP349, 121 more genes
    nsv7064729inversion1nstd229human GRCh38 chr11: 102,706,869-103,032,485 , GRCh37.p13 chr11: 102,577,600-102,903,214 CSNK1A1P2, WTAPP1, 9 more genes
    nsv7061741inversion1nstd229human GRCh38 chr11: 100,793,881-105,425,000 , GRCh37.p13 chr11: 100,664,612-105,295,727 MTND1P36, LOC102723862, 75 more genes
    nsv6915244copy number variation1nstd229human GRCh38 chr11: 102,837,741-102,837,773 , GRCh37.p13 chr11|NW_003871077.1: 5,976-6,008 , GRCh37.p13 chr11: 102,708,472-102,708,504 MMP3
    nsv6905056copy number variation1nstd229human GRCh38 chr11: 102,838,526-102,841,766 , GRCh37.p13 chr11|NW_003871077.1: 6,761-10,001 , GRCh37.p13 chr11: 102,709,257-102,712,497 MMP3
    nsv6904670copy number variation1nstd229human GRCh38 chr11: 102,830,151-102,845,125 , GRCh37.p13 chr11: 102,702,497-102,715,856 , GRCh37.p13 chr11|NW_003871077.1: 1-13,360 MMP3, WTAPP1
    nsv6898519copy number variation1nstd229human GRCh38 chr11: 101,614,768-102,883,244 , GRCh37.p13 chr11: 101,485,499-102,702,496 PLS1P1, MMP3, 26 more genes
    nsv6637687copy number variation1nstd102humanPathogenic GRCh37 chr11: 101,371,503-109,306,519 , GRCh38.p12 chr11: 101,500,772-109,435,793 GRIA4, MTND1P36, 111 more genes
    nsv6637671copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 98,770,072-104,602,846 , GRCh38.p12 chr11: 98,899,342-104,732,118 BIRC2, BIRC3, 67 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6637174copy number variation1nstd102humanUncertain significance GRCh37 chr11: 99,059,204-103,281,943 , GRCh38.p12 chr11: 99,188,473-103,411,215 TMEM123, LOC100418997, 55 more genes
    nsv6582485inversion1nstd223human GRCh38 chr11: 100,023,537-103,679,304 , GRCh37.p13 chr11: 99,894,269-103,550,032 BOLA3P1, LOC100190922, 56 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6309019copy number variation2nstd102humanPathogenic GRCh37 chr11: 101,323,686-103,349,981 , GRCh38.p12 chr11: 101,452,955-103,479,253 RPL21P96, RNU6-952P, 40 more genes
    nsv6301083copy number variation1nstd186human GRCh37 chr11: 102,707,993-102,709,431 , GRCh38.p12 chr11: 102,837,262-102,838,700 MMP3, WTAPP1
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 more genes
    nsv6132066copy number variation1nstd213human GRCh37 chr11: 101,180,000-103,180,001 , GRCh38.p12 chr11: 101,309,269-103,309,272 BIRC2, MMP3, 35 more genes
    nsv6131906copy number variation1nstd213human GRCh37 chr11: 102,640,000-102,710,001 , GRCh38.p12 chr11: 102,769,269-102,839,270 MMP1, MMP3, 3 more genes
    nsv6093959insertion1nstd212human GRCh38 chr11: 102,834,216-102,834,216 , GRCh37.p13 chr11|NW_003871077.1: 2,451-2,451 , GRCh37.p13 chr11: 102,704,947-102,704,947 MMP3, WTAPP1
    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