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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068381inversion1nstd229human GRCh38 chr12: 9,995,330-10,124,025 , GRCh37.p13 chr12: 10,147,929-10,276,624 CLEC7A, RN7SKP161, 9 more genes
    nsv7068010inversion1nstd229human GRCh38 chr12: 7,025,778-10,225,656 , GRCh37.p13 chr12: 7,178,850-10,378,255 GOT2P3, CLEC2B, 123 more genes
    nsv7064008inversion1nstd229human GRCh38 chr12: 6,716,253-10,225,825 , GRCh37.p13 chr12: 6,825,419-10,378,424 PTMAP4, COPS7A, 153 more genes
    nsv6928671copy number variation1nstd229human GRCh38 chr12: 10,002,001-10,007,900 , GRCh37.p13 chr12: 10,154,600-10,160,499 CLEC1B, CLEC12B
    nsv6928130copy number variation1nstd229human GRCh38 chr12: 9,986,637-9,998,535 , GRCh37.p13 chr12: 10,139,236-10,151,134 CLEC1B, CLEC12A
    nsv6925208copy number variation1nstd229human GRCh38 chr12: 9,940,016-9,995,473 , GRCh37.p13 chr12: 10,092,615-10,148,072 CLEC12A, LINC02470, 2 more genes
    nsv6637726copy number variation1nstd102humanUncertain significance GRCh37 chr12: 10,049,346-10,322,120 , GRCh38.p12 chr12: 9,896,747-10,169,521 CLEC1B, LOC102724020, 14 more genes
    nsv6589801inversion1nstd223human GRCh38 chr12: 9,986,296-9,986,421 , GRCh37.p13 chr12: 10,138,895-10,139,020 CLEC12A, CLEC1B
    nsv6456183copy number variation1nstd223human GRCh38 chr12: 9,964,309-10,014,216 , GRCh37.p13 chr12: 10,116,908-10,166,815 CLEC12A, LOC102724020, 2 more genes
    nsv6292259mobile element insertion1nstd186human GRCh37 chr12: 10,138,521-10,138,572 , GRCh38.p12 chr12: 9,985,922-9,985,973 CLEC1B, CLEC12A
    nsv6240653mobile element insertion1nstd215human GRCh38 chr12: 9,996,556-9,996,556 , GRCh37.p13 chr12: 10,149,155-10,149,155 CLEC1B
    nsv6240652mobile element insertion1nstd215human GRCh38 chr12: 9,985,922-9,985,922 , GRCh37.p13 chr12: 10,138,521-10,138,521 CLEC1B, CLEC12A
    nsv6132723copy number variation1nstd213human GRCh37 chr12: 9,810,000-10,140,001 , GRCh38.p12 chr12: 9,657,404-9,987,402 CD69, CLECL1P, 13 more genes
    nsv6132720copy number variation1nstd213human GRCh37 chr12: 9,040,000-17,930,001 , GRCh38.p12 chr12: 8,887,404-17,777,067 A2M, A2MP1, 215 more genes
    nsv6132616copy number variation1nstd213human GRCh37 chr12: 8,100,000-12,900,001 , GRCh38.p12 chr12: 7,947,404-12,747,067 A2M, A2MP1, 178 more genes
    nsv6132518copy number variation1nstd213human GRCh37 chr12: 9,010,000-10,480,001 , GRCh38.p12 chr12: 8,857,404-10,327,402 CD69, CLEC1A, 56 more genes
    nsv6132445copy number variation1nstd213human GRCh37 chr12: 9,040,000-11,190,001 , GRCh38.p12 chr12: 8,887,404-11,037,402 A2M, A2MP1, 95 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
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