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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv6911487copy number variation1nstd229human GRCh38 chr11: 130,553,739-131,533,260 , GRCh37.p13 chr11: 130,423,634-131,403,154 LOC105369579, LOC107984412, 15 more genes
    nsv6905918copy number variation1nstd229human GRCh38 chr11: 130,720,239-131,215,051 , GRCh37.p13 chr11: 130,590,134-131,084,946 LOC105369575, PPP1R10P1, 9 more genes
    nsv6904413copy number variation1nstd229human GRCh38 chr11: 130,829,756-130,947,650 , GRCh37.p13 chr11: 130,699,651-130,817,545 LINC02551, SNX19
    nsv6903212copy number variation1nstd229human GRCh38 chr11: 130,855,971-130,861,739 , GRCh37.p13 chr11: 130,725,866-130,731,634 LINC02551
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6634467copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 127,074,235-135,006,516 , GRCh38.p12 chr11: 127,204,340-135,076,622 APLP2, BAK1P2, 98 more genes
    nsv6467315copy number variation1nstd223human GRCh38 chr11: 130,553,739-131,533,260 , GRCh37.p13 chr11: 130,423,634-131,403,154 LOC105369577, LOC105369574, 15 more genes
    nsv6467171copy number variation1nstd223human GRCh38 chr11: 130,720,235-131,215,048 , GRCh37.p13 chr11: 130,590,130-131,084,943 LOC107984411, LOC105369575, 9 more genes
    nsv6464426copy number variation1nstd223human GRCh38 chr11: 130,853,251-130,853,737 , GRCh37.p13 chr11: 130,723,146-130,723,632 LINC02551
    nsv6462284copy number variation1nstd223human GRCh38 chr11: 130,563,109-131,175,248 , GRCh37.p13 chr11: 130,433,004-131,045,143 LOC105369577, PPP1R10P1, 10 more genes
    nsv6458339copy number variation1nstd223human GRCh38 chr11: 130,862,421-130,862,965 , GRCh37.p13 chr11: 130,732,316-130,732,860 LINC02551
    nsv6457228copy number variation1nstd223human GRCh38 chr11: 130,844,791-130,849,034 , GRCh37.p13 chr11: 130,714,686-130,718,929 LINC02551
    nsv6315559copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 130,173,156-134,938,470 , GRCh38.p12 chr11: 130,303,261-135,068,576 BAK1P2, OPCML, 54 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
    nsv6315090copy number variation1nstd102humanPathogenic GRCh37 chr11: 128,634,685-134,257,741 , GRCh38.p12 chr11: 128,764,790-134,387,847 BAK1P2, RN7SL167P, 73 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv6132085copy number variation1nstd213human GRCh37 chr11: 130,710,000-134,940,001 , GRCh38.p12 chr11: 130,840,105-135,070,107 PTP4A2P2, NCAPD3, 42 more genes
    nsv5911858copy number variation1nstd209human GRCh38 chr11: 130,566,993-131,257,127 , GRCh37.p13 chr11: 130,436,888-131,127,022 PPP1R10P1, LINC02551, 11 more genes
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