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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147125insertion1nstd232human GRCh37.p13 chr11: 102,272,939-102,272,939 , GRCh38.p12 chr11: 102,402,208-102,402,208 TMEM123
    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
    nsv7062751inversion1nstd229human GRCh38 chr11: 102,451,481-102,452,969 , GRCh37.p13 chr11: 102,322,212-102,323,700 TMEM123, TMEM123-DT
    nsv7061741inversion1nstd229human GRCh38 chr11: 100,793,881-105,425,000 , GRCh37.p13 chr11: 100,664,612-105,295,727 MTND1P36, LOC102723862, 75 more genes
    nsv6916266copy number variation1nstd229human GRCh38 chr11: 102,395,265-102,405,490 , GRCh37.p13 chr11: 102,265,996-102,276,221 TMEM123
    nsv6915092copy number variation1nstd229human GRCh38 chr11: 102,445,986-102,446,210 , GRCh37.p13 chr11: 102,316,717-102,316,941 TMEM123
    nsv6910682copy number variation1nstd229human GRCh38 chr11: 102,449,463-102,546,323 , GRCh37.p13 chr11: 102,320,194-102,417,054 LOC102723838, TMEM123, 2 more genes
    nsv6906703copy number variation1nstd229human GRCh38 chr11: 102,408,729-102,418,566 , GRCh37.p13 chr11: 102,279,460-102,289,297 TMEM123
    nsv6904906copy number variation1nstd229human GRCh38 chr11: 102,396,969-102,397,001 , GRCh37.p13 chr11: 102,267,700-102,267,732 TMEM123
    nsv6901800copy number variation1nstd229human GRCh38 chr11: 102,432,857-102,436,759 , GRCh37.p13 chr11: 102,303,588-102,307,490 TMEM123
    nsv6900922copy number variation1nstd229human GRCh38 chr11: 102,404,852-102,405,304 , GRCh37.p13 chr11: 102,275,583-102,276,035 TMEM123
    nsv6900060copy number variation1nstd229human GRCh38 chr11: 102,400,895-102,404,804 , GRCh37.p13 chr11: 102,271,626-102,275,535 TMEM123
    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
    nsv6593446inversion1nstd223human GRCh38 chr11: 102,404,853-102,406,615 , GRCh37.p13 chr11: 102,275,584-102,277,346 TMEM123
    nsv6582485inversion1nstd223human GRCh38 chr11: 100,023,537-103,679,304 , GRCh37.p13 chr11: 99,894,269-103,550,032 BOLA3P1, LOC100190922, 56 more genes
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