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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
    nsv7068895inversion1nstd229human GRCh38 chr11: 100,518,680-109,308,656 , GRCh37.p13 chr11: 100,389,411-109,179,383 LINC02719, RNA5SP349, 121 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
    nsv6914349copy number variation1nstd229human GRCh38 chr11: 102,584,101-102,587,900 , GRCh37.p13 chr11: 102,454,832-102,458,631 MMP20
    nsv6913833copy number variation1nstd229human GRCh38 chr11: 102,609,201-102,678,700 , GRCh37.p13 chr11: 102,479,932-102,549,431 MMP20, MMP20-AS1
    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
    nsv6912058copy number variation1nstd229human GRCh38 chr11: 102,593,001-102,617,300 , GRCh37.p13 chr11: 102,463,732-102,488,031 MMP20, MMP20-AS1
    nsv6911592copy number variation1nstd229human GRCh38 chr11: 102,595,143-102,599,946 , GRCh37.p13 chr11: 102,465,874-102,470,677 MMP20
    nsv6910034copy number variation1nstd229human GRCh38 chr11: 102,557,001-102,587,700 , GRCh37.p13 chr11: 102,427,732-102,458,431 MMP20
    nsv6908101copy number variation1nstd229human GRCh38 chr11: 102,614,872-102,694,893 , GRCh37.p13 chr11: 102,485,603-102,565,624 MMP20-AS1, MMP20, 1 more genes
    nsv6905567copy number variation1nstd229human GRCh38 chr11: 102,601,127-102,601,433 , GRCh37.p13 chr11: 102,471,858-102,472,164 MMP20
    nsv6900311copy number variation1nstd229human GRCh38 chr11: 102,615,830-102,636,011 , GRCh37.p13 chr11: 102,486,561-102,506,742 MMP20-AS1, MMP20
    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
    nsv6636030copy number variation1nstd102humanUncertain significance GRCh38 chr11: 102,601,121-102,601,432 , GRCh37 chr11: 102,471,852-102,472,163 MMP20
    nsv6582485inversion1nstd223human GRCh38 chr11: 100,023,537-103,679,304 , GRCh37.p13 chr11: 99,894,269-103,550,032 BOLA3P1, LOC100190922, 56 more genes
    nsv6474274copy number variation1nstd223human GRCh38 chr11: 102,601,127-102,601,431 , GRCh37.p13 chr11: 102,471,858-102,472,162 MMP20
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