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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5851049copy number variation2nstd209human GRCh38 chr12: 113,387,219-113,388,218 , GRCh37.p13 chr12: 113,825,024-113,826,023 PLBD2
    nsv5584673copy number variation1nstd207human GRCh38 chr12: 113,386,291-113,386,455 , GRCh37.p13 chr12: 113,824,096-113,824,260 PLBD2
    nsv5504338copy number variation1nstd206human GRCh38 chr12: 113,359,333-113,362,417 , GRCh37.p13 chr12: 113,797,138-113,800,222 LOC105369989, PLBD2
    nsv4995700copy number variation1nstd200human GRCh38 chr12: 113,363,335-113,369,944 , GRCh37.p13 chr12: 113,801,140-113,807,749 PLBD2
    nsv4995699copy number variation1nstd200human GRCh38 chr12: 113,363,056-113,365,509 , GRCh37.p13 chr12: 113,800,861-113,803,314 PLBD2
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 ACACB, ACADS, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 ACACB, ACADS, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 ACACB, ACADS, 452 more genes
    nsv4747461copy number variation1nstd199human GRCh37 chr12: 113,824,157-113,824,321 , GRCh38.p12 chr12: 113,386,352-113,386,516 PLBD2
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 RNA5SP368, LINC02555, 1787 more genes
    nsv4575252mobile element insertion1nstd166human GRCh37.p13 chr12: 113,813,122-113,813,122 , GRCh38.p12 chr12: 113,375,317-113,375,317 PLBD2
    nsv4456436copy number variation1nstd102humanUncertain significance GRCh37 chr12: 113,695,889-113,904,780 , GRCh38.p12 chr12: 113,258,084-113,466,975 SDS, TPCN1, 7 more genes
    nsv4380311copy number variation1nstd173human GRCh37 chr12: 113,628,648-113,905,101 , GRCh38.p12 chr12: 113,190,843-113,467,296 IQCD, MIR6762, 9 more genes
    nsv4374351copy number variation1nstd173human GRCh37 chr12: 113,630,747-113,904,780 , GRCh38.p12 chr12: 113,192,942-113,466,975 SLC8B1, SDSL, 8 more genes
    nsv4365342copy number variation2nstd173human GRCh37 chr12: 113,628,648-113,923,854 , GRCh38.p12 chr12: 113,190,843-113,486,049 LOC107984436, SDS, 10 more genes
    nsv4226974copy number variation1nstd166human GRCh37.p13 chr12: 113,805,984-113,814,767 , GRCh38.p12 chr12: 113,368,179-113,376,962 PLBD2
    nsv4222843copy number variation1nstd166human GRCh37.p13 chr12: 113,790,660-113,816,722 , GRCh38.p12 chr12: 113,352,855-113,378,917 PLBD2, LOC105369989
    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, 28 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 GLYCAM1, LOC101927436, 2523 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 RAN, LOC100506606, 2524 more genes
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