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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5970483insertion1nstd209human GRCh38 chr12: 122,121,010-122,121,010 , GRCh37.p13 chr12: 122,605,557-122,605,557 MLXIP
    nsv5940992copy number variation1nstd209human GRCh38 chr12: 122,094,623-122,094,760 , GRCh37.p13 chr: NaN-NaN MLXIP
    nsv5939690copy number variation1nstd209human GRCh38 chr12: 122,124,329-122,124,411 , GRCh37.p13 chr12: 122,608,876-122,608,958 MLXIP
    nsv5939613copy number variation1nstd209human GRCh38 chr12: 122,124,162-122,124,413 , GRCh37.p13 chr12: 122,608,709-122,608,960 MLXIP
    nsv5586617copy number variation1nstd207human GRCh38 chr12: 122,124,331-122,124,413 , GRCh37.p13 chr12: 122,608,878-122,608,960 MLXIP
    nsv5356470translocation1nstd200human GRCh38 chr12: 122,094,460-122,094,460 , GRCh38 chr12: 122,093,640-122,093,640 , GRCh37.p13 chr: NaN-NaN , GRCh37.p13 chr: NaN-NaN MLXIP
    nsv5355489translocation1nstd200human GRCh38 chr11: 133,354,203-133,354,203 , GRCh38 chr12: 122,093,711-122,093,711 , GRCh37.p13 chr: NaN-NaN , GRCh37.p13 chr11: 133,224,098-133,224,098 OPCML, MLXIP
    nsv5127195mobile element insertion1nstd203human GRCh38 chr12: 122,124,876-122,124,886 , GRCh37.p13 chr12: 122,609,423-122,609,433 MLXIP
    nsv4993793copy number variation1nstd200human GRCh38 chr12: 122,134,497-122,150,166 , GRCh37.p13 chr12: 122,619,044-122,634,713 MLXIP
    nsv4993792copy number variation1nstd200human GRCh38 chr12: 122,044,254-122,133,685 , GRCh37.p13 chr12: 122,482,160-122,618,232 MLXIP, LINC02985, 1 more genes
    nsv4842186copy number variation1nstd200human GRCh37 chr12: 122,619,044-122,634,713 , GRCh38.p12 chr12: 122,134,497-122,150,166 , GRCh38.p12 chr12|NW_011332697.1: 75,454-86,581 MLXIP
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
    nsv4736979copy number variation1nstd199human GRCh37 chr12: 122,608,722-122,608,817 , GRCh38.p12 chr12: 122,124,175-122,124,270 , GRCh38.p12 chr12|NW_011332697.1: 65,132-65,227 MLXIP
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4680254copy number variation1nstd189human GRCh37.p13 chr12: 121,825,920-122,679,071 , GRCh38.p12 chr12: 121,388,117-122,194,524 , BCL7A, 22 more genes
    nsv4614084copy number variation1nstd183human GRCh37 chr12: 122,627,371-122,687,925 , GRCh38.p12 chr12: 122,142,824-122,203,378 IL31, MLXIP, 2 more genes
    nsv4512522mobile element insertion1nstd166human GRCh37.p13 chr12: 122,623,746-122,623,746 , GRCh38.p12 chr12|NW_011332697.1: 80,156-80,156 , GRCh38.p12 chr12: 122,139,199-122,139,199 MLXIP
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