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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940778copy number variation1nstd209human GRCh38 chr12: 113,765,582-113,765,687 , GRCh37.p13 chr12: 114,203,387-114,203,492 LINC01234
    nsv5508005copy number variation1nstd206human GRCh38 chr12: 113,762,554-113,762,751 , GRCh37.p13 chr12: 114,200,359-114,200,556 LINC01234
    nsv5506496copy number variation1nstd206human GRCh38 chr12: 113,760,643-113,760,696 , GRCh37.p13 chr12: 114,198,448-114,198,501 LINC01234
    nsv5196395mobile element insertion1nstd203human GRCh38 chr12: 113,746,692-113,746,707 , GRCh37.p13 chr12: 114,184,497-114,184,512 LINC01234
    nsv4995709copy number variation1nstd200human GRCh38 chr12: 113,755,029-113,760,949 , GRCh37.p13 chr12: 114,192,834-114,198,754 LINC01234
    nsv4844587copy number variation1nstd200human GRCh37 chr12: 114,192,834-114,198,754 , GRCh38.p12 chr12: 113,755,029-113,760,949 LINC01234
    nsv4831040copy number variation1nstd200human GRCh37 chr12: 114,196,749-114,197,340 , GRCh38.p12 chr12: 113,758,944-113,759,535 LINC01234
    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
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4577479mobile element insertion1nstd166human GRCh37.p13 chr12: 114,185,599-114,185,599 , GRCh38.p12 chr12: 113,747,794-113,747,794 LINC01234
    nsv4225837copy number variation1nstd166human GRCh37.p13 chr12: 114,183,458-114,184,053 , GRCh38.p12 chr12: 113,745,653-113,746,248 LINC01234
    nsv4225144copy number variation1nstd166human GRCh37.p13 chr12: 114,201,079-114,201,397 , GRCh38.p12 chr12: 113,763,274-113,763,592 LINC01234
    nsv4214939copy number variation1nstd166human GRCh37.p13 chr12: 114,199,523-114,199,584 , GRCh38.p12 chr12: 113,761,718-113,761,779 LINC01234
    nsv3914285copy number variation1nstd102humanPathogenic GRCh38 chr12: 113,077,775-114,372,366 , NCBI36 chr12: 111,999,963-113,294,554 , GRCh37 chr12: 113,515,580-114,810,171 RITA1, DTX1, 27 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
    nsv3905255copy number variation1nstd102humanUncertain significance GRCh37 chr12: 114,103,287-114,656,460 , GRCh38.p12 chr12: 113,665,482-114,218,655 DYNLL1P4, LOC105369993, 7 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 , OR5BT1P, 2441 more genes
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