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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6915014copy number variation1nstd229human GRCh38 chr11: 76,397,854-76,401,892 , GRCh37.p13 chr11: 76,108,898-76,112,936 GVQW3
    nsv6914464copy number variation1nstd229human GRCh38 chr11: 76,405,969-76,409,432 , GRCh37.p13 chr11: 76,117,013-76,120,476 GVQW3
    nsv6911095copy number variation1nstd229human GRCh38 chr11: 76,397,022-76,406,565 , GRCh37.p13 chr11: 76,108,066-76,117,609 GVQW3
    nsv6908419copy number variation1nstd229human GRCh38 chr11: 76,396,565-76,400,365 , GRCh37.p13 chr11: 76,107,609-76,111,409 GVQW3
    nsv6904918copy number variation1nstd229human GRCh38 chr11: 76,390,566-76,397,755 , GRCh37.p13 chr11: 76,101,610-76,108,799 GVQW3
    nsv6592362inversion1nstd223human GRCh38 chr11: 76,383,778-76,384,340 , GRCh37.p13 chr11: 76,094,822-76,095,384 GVQW3
    nsv6591675inversion1nstd223human GRCh38 chr11: 76,397,900-76,398,604 , GRCh37.p13 chr11: 76,108,944-76,109,648 GVQW3
    nsv6588046inversion1nstd223human GRCh38 chr11: 76,397,989-76,398,540 , GRCh37.p13 chr11: 76,109,033-76,109,584 GVQW3
    nsv6587609inversion1nstd223human GRCh38 chr11: 76,402,428-76,403,098 , GRCh37.p13 chr11: 76,113,472-76,114,142 GVQW3
    nsv6583433inversion1nstd223human GRCh38 chr11: 76,383,839-76,384,308 , GRCh37.p13 chr11: 76,094,883-76,095,352 GVQW3
    nsv6465370copy number variation1nstd223human GRCh38 chr11: 76,380,101-76,382,300 , GRCh37.p13 chr11: 76,091,145-76,093,344 GVQW3, THAP12
    nsv6457337copy number variation1nstd223human GRCh38 chr11: 76,396,562-76,400,361 , GRCh37.p13 chr11: 76,107,606-76,111,405 GVQW3
    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
    nsv6301673copy number variation1nstd186human GRCh37 chr11: 76,097,915-76,098,083 , GRCh38.p12 chr11: 76,386,871-76,387,039 GVQW3
    nsv6095728insertion1nstd212human GRCh38 chr11: 76,408,118-76,408,118 , GRCh37.p13 chr11: 76,119,162-76,119,162 GVQW3
    nsv5505007copy number variation1nstd206human GRCh38 chr11: 76,386,871-76,387,039 , GRCh37.p13 chr11: 76,097,915-76,098,083 GVQW3
    nsv5493982copy number variation1nstd206human GRCh38 chr11: 76,405,505-76,413,460 , GRCh37.p13 chr11: 76,116,549-76,124,504 GVQW3
    nsv5493955copy number variation1nstd206human GRCh38 chr11: 76,396,593-76,400,361 , GRCh37.p13 chr11: 76,107,637-76,111,405 GVQW3
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5363222translocation1nstd200human GRCh38 chr11: 76,381,132-76,381,132 , GRCh38 chr6: 90,590,715-90,590,715 , GRCh37.p13 chr11: 76,092,176-76,092,176 , GRCh37.p13 chr6: 91,300,434-91,300,434 GVQW3, THAP12
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