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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5968724inversion1nstd209human GRCh38 chr12: 6,473,720-6,709,618 , GRCh37.p13 chr12: 6,582,886-6,818,784 CHD4, GAPDH, 15 more genes
    nsv5913026copy number variation1nstd209human GRCh38 chr12: 6,634,993-6,635,093 , GRCh37.p13 chr12: 6,744,159-6,744,259 LPAR5
    nsv5564211copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-7,362,819 , GRCh38.p12 chr12: 6,329,312-7,210,223 GPR162, SCARNA11, 68 more genes
    nsv5510830copy number variation1nstd206human GRCh38 chr12: 6,631,540-6,631,599 , GRCh37.p13 chr12: 6,740,706-6,740,765 LPAR5
    nsv5501149copy number variation1nstd206human GRCh38 chr12: 6,627,331-6,629,172 , GRCh37.p13 chr12: 6,736,497-6,738,338 LOC105369631, LPAR5
    nsv5348540translocation1nstd200human GRCh38 chr12: 6,622,274-6,622,274 , GRCh38 chr12: 6,622,336-6,622,336 , GRCh37.p13 chr12: 6,731,502-6,731,502 , GRCh37.p13 chr12: 6,731,440-6,731,440 LPAR5, LOC105369631
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5316979copy number variation1nstd204human GRCh37.p13 chr12: 6,736,502-6,738,289 , GRCh38.p13 chr12: 6,627,336-6,629,123 LPAR5, LOC105369631
    nsv5279702copy number variation1nstd204human GRCh38.p13 chr12: 6,507,601-6,909,400 , GRCh37.p13 chr12: 6,616,767-6,907,580 ING4, LPAR5, 30 more genes
    nsv5129782mobile element insertion1nstd203human GRCh38 chr12: 6,622,348-6,622,384 , GRCh37.p13 chr12: 6,731,514-6,731,550 LOC105369631, LPAR5
    nsv4972012copy number variation1nstd200human GRCh38 chr12: 6,634,910-6,649,166 , GRCh37.p13 chr12: 6,744,076-6,758,332 ACRBP, ING4, 1 more genes
    nsv4972011copy number variation1nstd200human GRCh38 chr12: 6,629,128-6,629,238 , GRCh37.p13 chr12: 6,738,294-6,738,404 LPAR5
    nsv4972010copy number variation1nstd200human GRCh38 chr12: 6,627,469-6,629,531 , GRCh37.p13 chr12: 6,736,635-6,738,697 LPAR5, LOC105369631
    nsv4972009copy number variation1nstd200human GRCh38 chr12: 6,627,388-6,629,119 , GRCh37.p13 chr12: 6,736,554-6,738,285 LOC105369631, LPAR5
    nsv4972008copy number variation1nstd200human GRCh38 chr12: 6,622,317-6,626,117 , GRCh37.p13 chr12: 6,731,483-6,735,283 LPAR5, LOC105369631
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4848019copy number variation1nstd200human GRCh37 chr12: 6,744,076-6,758,332 , GRCh38.p12 chr12: 6,634,910-6,649,166 ACRBP, ING4, 1 more genes
    nsv4842362copy number variation1nstd200human GRCh37 chr12: 6,736,502-6,738,290 , GRCh38.p12 chr12: 6,627,336-6,629,124 LOC105369631, LPAR5
    nsv4841876copy number variation1nstd200human GRCh37 chr12: 6,737,456-6,738,350 , GRCh38.p12 chr12: 6,628,290-6,629,184 LPAR5
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