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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143077copy number variation1nstd232human GRCh37.p13 chr12: 40,540,535-40,540,606 , GRCh38.p12 chr12: 40,146,733-40,146,804 LINC02555
    nsv7069491inversion1nstd229human GRCh38 chr12: 38,629,739-41,866,812 , GRCh37.p13 chr12: 39,023,541-42,260,614 CPNE8, LOC100421126, 29 more genes
    nsv6936185copy number variation1nstd229human GRCh38 chr12: 39,947,509-40,184,009 , GRCh37.p13 chr12: 40,341,311-40,577,811 LINC02555, SLC2A13, 3 more genes
    nsv6934101copy number variation1nstd229human GRCh38 chr12: 39,893,726-40,431,148 , GRCh37.p13 chr12: 40,287,528-40,824,950 LINC02555, LOC105369735, 9 more genes
    nsv6924073copy number variation1nstd229human GRCh38 chr12: 40,129,525-40,668,745 , GRCh37.p13 chr12: 40,523,327-41,062,547 LINC02471, RNU6-713P, 7 more genes
    nsv6923657copy number variation1nstd229human GRCh38 chr12: 38,729,378-41,761,232 , GRCh37.p13 chr12: 39,123,180-42,155,034 RPL30P13, LOC100421126, 28 more genes
    nsv6920972copy number variation1nstd229human GRCh38 chr12: 39,183,535-40,190,313 , GRCh37.p13 chr12: 39,577,337-40,584,115 REDIC1, LINC02471, 9 more genes
    nsv6919749copy number variation1nstd229human GRCh38 chr12: 39,639,819-40,952,818 , GRCh37.p13 chr12: 40,033,621-41,346,620 LINC02471, RNU6-713P, 14 more genes
    nsv6637982copy number variation1nstd102humanUncertain significance GRCh37 chr12: 39,560,669-43,285,298 , GRCh38.p12 chr12: 39,166,867-42,891,495 RPS27P21, LINC02471, 41 more genes
    nsv6591997inversion1nstd223human GRCh38 chr12: 38,629,735-41,866,813 , GRCh37.p13 chr12: 39,023,537-42,260,615 LOC100420117, LINC02400, 29 more genes
    nsv6470829copy number variation1nstd223human GRCh38 chr12: 39,968,932-41,209,513 , GRCh37.p13 chr12: 40,362,734-41,603,315 LRRK2-DT, LRRK2, 13 more genes
    nsv6470498copy number variation1nstd223human GRCh38 chr12: 40,160,055-40,171,622 , GRCh37.p13 chr12: 40,553,857-40,565,424 LINC02555, LINC02471
    nsv6468779copy number variation1nstd223human GRCh38 chr12: 40,140,901-40,141,600 , GRCh37.p13 chr12: 40,534,703-40,535,402 LINC02555
    nsv6461696copy number variation1nstd223human GRCh38 chr12: 40,142,801-40,144,000 , GRCh37.p13 chr12: 40,536,603-40,537,802 LINC02555
    nsv6458191copy number variation1nstd223human GRCh38 chr12: 40,151,601-40,152,700 , GRCh37.p13 chr12: 40,545,403-40,546,502 LINC02555
    nsv6456486copy number variation1nstd223human GRCh38 chr12: 40,139,606-40,146,037 , GRCh37.p13 chr12: 40,533,408-40,539,839 LINC02555
    nsv6287971insertion1nstd214human GRCh38 chr12: 40,146,234-40,146,234 , GRCh37.p13 chr12: 40,540,036-40,540,036 LINC02555
    nsv6191554copy number variation1nstd214human GRCh38 chr12: 40,146,771-40,146,821 , GRCh37.p13 chr12: 40,540,573-40,540,623 LINC02555
    nsv6132695copy number variation1nstd213human GRCh37 chr12: 37,860,000-42,780,001 , GRCh38.p12 chr12: 37,466,198-42,386,199 PDZRN4, SLC2A13, 48 more genes
    nsv6132337copy number variation1nstd213human GRCh37 chr12: 39,860,000-40,820,001 , GRCh38.p12 chr12: 39,466,198-40,426,199 SLC2A13, REDIC1, 11 more genes
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