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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946347copy number variation1nstd209human GRCh38 chr12: 49,095,436-49,095,594 , GRCh37.p13 chr12: 49,489,219-49,489,377 LMBR1L, LOC105369759
    nsv5709682mobile element insertion1nstd211human GRCh38 chr12: 49,098,062-49,098,062 , GRCh37.p13 chr12: 49,491,845-49,491,845 LMBR1L
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
    nsv5553127insertion1nstd206human GRCh38 chr12: 49,100,926-49,100,926 , GRCh37.p13 chr12: 49,494,709-49,494,709 LMBR1L
    nsv5513026copy number variation1nstd206human GRCh38 chr12: 49,099,502-49,107,978 , GRCh37.p13 chr12: 49,493,285-49,501,761 LMBR1L
    nsv5509459copy number variation1nstd206human GRCh38 chr12: 49,095,437-49,095,595 , GRCh37.p13 chr12: 49,489,220-49,489,378 LOC105369759, LMBR1L
    nsv5427915mobile element insertion1nstd206human GRCh38 chr12: 49,098,062-49,098,113 , GRCh37.p13 chr12: 49,491,845-49,491,896 LMBR1L
    nsv5355895translocation1nstd200human GRCh38 chr12: 49,095,437-49,095,437 , GRCh38 chr12: 49,095,595-49,095,595 , GRCh37.p13 chr12: 49,489,220-49,489,220 , GRCh37.p13 chr12: 49,489,378-49,489,378 LOC105369759, LMBR1L
    nsv5330406translocation1nstd200human GRCh37 chr3: 153,294,218-153,294,218 , GRCh37 chr12: 49,494,712-49,494,712 , GRCh38.p12 chr3: 153,576,429-153,576,429 , GRCh38.p12 chr12: 49,100,929-49,100,929 LMBR1L, LINC02006
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv4972550copy number variation1nstd200human GRCh38 chr12: 49,108,237-49,122,743 , GRCh37.p13 chr12: 49,502,020-49,516,526 LMBR1L
    nsv4849266copy number variation1nstd200human GRCh37 chr12: 49,493,307-49,501,739 , GRCh38.p12 chr12: 49,099,524-49,107,956 LMBR1L
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754531insertion1nstd199human GRCh37 chr12: 49,494,705-49,494,705 , GRCh38.p12 chr12: 49,100,922-49,100,922 LMBR1L
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4728793copy number variation1nstd102humanUncertain significance GRCh37 chr12: 49,024,019-50,299,974 , GRCh38.p12 chr12: 48,630,236-49,906,191 SPATS2, SPMIP11, 62 more genes
    nsv4607428copy number variation1nstd183human GRCh37 chr12: 49,495,943-49,496,068 , GRCh38.p12 chr12: 49,102,160-49,102,285 LMBR1L
    nsv4599872copy number variation1nstd183human GRCh37 chr12: 49,495,894-49,495,987 , GRCh38.p12 chr12: 49,102,111-49,102,204 LMBR1L
    nsv4548532insertion1nstd166human GRCh37.p13 chr12: 49,494,709-49,494,709 , GRCh38.p12 chr12: 49,100,926-49,100,926 LMBR1L
    nsv4507493mobile element insertion1nstd166human GRCh37.p13 chr12: 49,499,926-49,499,926 , GRCh38.p12 chr12: 49,106,143-49,106,143 LMBR1L
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