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Items: 1 to 20 of 173

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    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
    nsv7072206inversion1nstd229human GRCh38 chr11: 102,719,414-102,720,483 , GRCh37.p13 chr11: 102,590,145-102,591,214 MMP8
    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
    nsv6917280copy number variation1nstd229human GRCh38 chr11: 102,722,870-102,726,263 , GRCh37.p13 chr11: 102,593,601-102,596,994 MMP8
    nsv6915224copy number variation1nstd229human GRCh38 chr11: 102,724,273-102,747,946 , GRCh37.p13 chr11: 102,595,004-102,618,677 MMP8
    nsv6913806copy number variation1nstd229human GRCh38 chr11: 102,590,001-102,734,000 , GRCh37.p13 chr11: 102,460,732-102,604,731 MMP8, MMP27, 2 more genes
    nsv6907116copy number variation1nstd229human GRCh38 chr11: 102,699,205-102,715,625 , GRCh37.p13 chr11: 102,569,936-102,586,356 MMP8, MMP27
    nsv6905704copy number variation1nstd229human GRCh38 chr11: 102,720,241-102,720,607 , GRCh37.p13 chr11: 102,590,972-102,591,338 MMP8
    nsv6903908copy number variation1nstd229human GRCh38 chr11: 102,711,420-102,711,577 , GRCh37.p13 chr11: 102,582,151-102,582,308 MMP8
    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
    nsv6620451copy number variation1nstd224human GRCh37 chr11: 102,595,135-102,624,914 , GRCh38.p12 chr11: 102,724,404-102,754,183 MMP8
    nsv6594401inversion1nstd223human GRCh38 chr11: 102,719,415-102,720,553 , GRCh37.p13 chr11: 102,590,146-102,591,284 MMP8
    nsv6582485inversion1nstd223human GRCh38 chr11: 100,023,537-103,679,304 , GRCh37.p13 chr11: 99,894,269-103,550,032 BOLA3P1, LOC100190922, 56 more genes
    nsv6472987copy number variation1nstd223human GRCh38 chr11: 102,711,101-102,711,900 , GRCh37.p13 chr11: 102,581,832-102,582,631 MMP8
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