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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5937329copy number variation1nstd209human GRCh38 chr12: 68,205,556-68,206,547 , GRCh37.p13 chr12: 68,599,336-68,600,327 LOC105369818, IL26
    nsv5127411mobile element insertion1nstd203human GRCh38 chr12: 68,210,338-68,210,338 , GRCh37.p13 chr12: 68,604,118-68,604,118 LOC105369818, IL26
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv4995104copy number variation1nstd200human GRCh38 chr12: 68,219,438-68,220,060 , GRCh37.p13 chr12: 68,613,218-68,613,840 LOC105369818, IL26
    nsv4995103copy number variation1nstd200human GRCh38 chr12: 68,211,126-68,211,378 , GRCh37.p13 chr12: 68,604,906-68,605,158 IL26, LOC105369818
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4845369copy number variation1nstd200human GRCh37 chr12: 68,613,218-68,613,840 , GRCh38.p12 chr12: 68,219,438-68,220,060 IL26, LOC105369818
    nsv4843351copy number variation1nstd200human GRCh37 chr12: 68,604,906-68,605,158 , GRCh38.p12 chr12: 68,211,126-68,211,378 IL26, LOC105369818
    nsv4839153copy number variation1nstd200human GRCh37 chr12: 68,619,375-68,619,594 , GRCh38.p12 chr12: 68,225,595-68,225,814 LOC105369818, IL26
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 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
    nsv4729265copy number variation1nstd102humanPathogenic GRCh37 chr12: 68,572,386-70,833,868 , GRCh38.p12 chr12: 68,178,606-70,440,088 LINC02384, LOC101928002, 47 more genes
    nsv4679187copy number variation1nstd189human GRCh37.p13 chr12: 68,540,821-68,666,480 , GRCh38.p12 chr12: 68,147,041-68,272,700 IFNG, IL22, 3 more genes
    nsv4617127copy number variation1nstd183human GRCh37 chr12: 68,619,113-68,619,235 , GRCh38.p12 chr12: 68,225,333-68,225,455 IL26, LOC105369818
    nsv4615770copy number variation1nstd183human GRCh37 chr12: 68,619,051-68,619,172 , GRCh38.p12 chr12: 68,225,271-68,225,392 LOC105369818, IL26
    nsv4564962mobile element insertion1nstd166human GRCh37.p13 chr12: 68,598,249-68,598,249 , GRCh38.p12 chr12: 68,204,469-68,204,469 IL26, LOC105369818
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