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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
    nsv6913329copy number variation1nstd229human GRCh38 chr11: 130,284,586-130,307,921 , GRCh37.p13 chr11: 130,154,481-130,177,816 ZBTB44, DDX18P5, 1 more genes
    nsv6907428copy number variation1nstd229human GRCh38 chr11: 130,111,862-130,301,154 , GRCh37.p13 chr11: 129,981,757-130,171,049 ST14, NDUFAF2P2, 3 more genes
    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
    nsv6583129inversion1nstd223human GRCh38 chr11: 130,283,211-130,283,941 , GRCh37.p13 chr11: 130,153,106-130,153,836 NDUFAF2P2, ZBTB44
    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
    nsv6132350copy number variation1nstd213human GRCh37 chr11: 128,570,000-130,240,001 , GRCh38.p12 chr11: 128,700,105-130,370,106 KCNJ1, ZBTB44, 28 more genes
    nsv5496017copy number variation1nstd206human GRCh38 chr11: 130,243,940-130,343,202 , GRCh37.p13 chr11: 130,113,835-130,213,097 RN7SL778P, ZBTB44, 3 more genes
    nsv5130474mobile element insertion1nstd203human GRCh38 chr11: 130,283,969-130,283,998 , GRCh37.p13 chr11: 130,153,864-130,153,893 ZBTB44, NDUFAF2P2
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4729098copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 130,128,323-134,938,470 , GRCh38.p12 chr11: 130,258,428-135,068,576 BAK1P2, OPCML, 56 more genes
    nsv4729012copy number variation1nstd102humanPathogenic GRCh37 chr11: 127,602,115-134,938,470 , GRCh38.p12 chr11: 127,732,220-135,068,576 LINC02706, APLP2, 92 more genes
    nsv4728891copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,785,487-134,938,470 , GRCh38.p12 chr11: 125,915,592-135,068,576 ARHGAP32, NAP1L1P1, 125 more genes
    nsv4675832copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576 MIR8052, BLID, 275 more genes
    nsv4675674copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,232,608-134,938,470 , GRCh38.p12 chr11: 124,362,712-135,068,576 FAM118B, PUS3, 184 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
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