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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074145inversion1nstd229human GRCh38 chr11: 104,112,094-113,544,164 , GRCh37.p13 chr11: 103,982,822-113,414,886 COLCA1, LOC105369491, 150 more genes
    nsv7069281inversion1nstd229human GRCh38 chr11: 107,936,485-114,400,629 , GRCh37.p13 chr11: 107,807,211-114,271,351 LRRC37A13P, POU2AF3, 121 more genes
    nsv7065935inversion1nstd229human GRCh38 chr11: 107,044,115-113,544,291 , GRCh37.p13 chr11: 106,914,841-113,415,013 LINC02762, TIMM8B, 112 more genes
    nsv6917023copy number variation1nstd229human GRCh38 chr11: 112,244,501-112,253,500 , GRCh37.p13 chr11: 112,115,224-112,124,223 PLET1
    nsv6902842copy number variation1nstd229human GRCh38 chr11: 112,238,376-112,248,794 , GRCh37.p13 chr11: 112,109,099-112,119,517 PLET1
    nsv6900237copy number variation1nstd229human GRCh38 chr11: 112,196,001-112,247,900 , GRCh37.p13 chr11: 112,066,724-112,118,623 RPS12P21, PTS, 4 more genes
    nsv6637811copy number variation1nstd102humanPathogenic GRCh37 chr11: 109,328,787-116,414,966 , GRCh38.p12 chr11: 109,458,061-116,544,249 LOC102723966, NXPE4, 129 more genes
    nsv6620697copy number variation1nstd224human GRCh37 chr11: 112,064,216-112,362,462 , GRCh38.p12 chr11: 112,193,493-112,491,739 MRPS36P4, PLET1, 12 more genes
    nsv6620695copy number variation1nstd224human GRCh37 chr11: 111,953,288-112,208,967 , GRCh38.p12 chr11: 112,082,564-112,338,244 TIMM8B, NKAPD1, 15 more genes
    nsv6586218inversion1nstd223human GRCh38 chr11: 107,936,497-114,408,912 , GRCh37.p13 chr11: 107,807,223-114,279,634 LOC107984390, ATF4P4, 121 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
    nsv6290834copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,422,071-118,022,671 , GRCh38.p12 chr11: 85,711,028-118,151,956 CARD17P, RNA5SP350, 480 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
    nsv6132074copy number variation1nstd213human GRCh37 chr11: 112,030,000-112,490,001 , GRCh38.p12 chr11: 112,159,277-112,619,278 BCO2, KCTD9P4, 17 more genes
    nsv6030277copy number variation1nstd212human GRCh38 chr11: 112,240,292-112,285,438 , GRCh37.p13 chr11: 112,111,015-112,156,161 LINC02762, PLET1, 2 more genes
    nsv6022475copy number variation1nstd212human GRCh38 chr11: 112,254,902-112,254,985 , GRCh37.p13 chr11: 112,125,625-112,125,708 PLET1
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 more genes
    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
    nsv4989302copy number variation1nstd200human GRCh38 chr11: 112,103,571-112,393,649 , GRCh37.p13 chr11: 111,974,295-112,264,372 , LINC02762, 14 more genes
    nsv4734137copy number variation1nstd199human GRCh37 chr11: 112,125,659-112,125,722 , GRCh38.p12 chr11: 112,254,936-112,254,999 PLET1
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