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Items: 1 to 20 of 194

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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
    nsv7073777inversion1nstd229human GRCh38 chr11: 126,864,523-126,951,110 , GRCh37.p13 chr11: 126,734,418-126,821,006 KIRREL3, KIRREL3-AS2, 1 more genes
    nsv7071859inversion1nstd229human GRCh38 chr11: 126,847,104-126,956,193 , GRCh37.p13 chr11: 126,716,999-126,826,089 KIRREL3-AS2, KIRREL3, 1 more genes
    nsv6912463copy number variation1nstd229human GRCh38 chr11: 126,864,501-126,948,600 , GRCh37.p13 chr11: 126,734,396-126,818,496 KIRREL3-AS2, KIRREL3, 1 more genes
    nsv6909979copy number variation1nstd229human GRCh38 chr11: 126,830,101-126,956,200 , GRCh37.p13 chr11: 126,699,996-126,826,096 LOC105369559, KIRREL3, 1 more genes
    nsv6904653copy number variation1nstd229human GRCh38 chr11: 126,936,781-126,943,162 , GRCh37.p13 chr11: 126,806,677-126,813,058 LOC105369559, KIRREL3, 1 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
    nsv6459462copy number variation1nstd223human GRCh38 chr11: 126,651,572-128,129,487 , GRCh37.p13 chr11: 126,521,467-127,999,382 KIRREL3-AS2, LINC02712, 16 more genes
    nsv6455795copy number variation1nstd223human GRCh38 chr11: 126,936,781-126,943,159 , GRCh37.p13 chr11: 126,806,677-126,813,055 LOC105369559, KIRREL3, 1 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
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 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
    nsv6132082copy number variation1nstd213human GRCh37 chr11: 126,220,000-126,870,001 , GRCh38.p12 chr11: 126,350,105-127,000,105 MIR3167, KIRREL3-AS2, 8 more genes
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 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
    nsv4676037copy number variation1nstd102humanUncertain significance GRCh37 chr11: 126,734,337-126,944,508 , GRCh38.p12 chr11: 126,864,442-127,074,613 LOC105369558, KIRREL3-AS2, 5 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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