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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143260insertion1nstd232human GRCh37.p13 chr12: 46,293,477-46,293,477 , GRCh38.p12 chr12: 45,899,694-45,899,694 ARID2
    nsv7077316inversion1nstd229human GRCh38 chr12: 45,864,161-45,864,266 , GRCh37.p13 chr12: 46,257,944-46,258,049 ARID2
    nsv7066444inversion1nstd229human GRCh38 chr12: 45,848,799-45,848,910 , GRCh37.p13 chr12: 46,242,582-46,242,693 LOC105369745, ARID2
    nsv6937664copy number variation1nstd229human GRCh38 chr12: 45,773,319-45,784,620 , GRCh37.p13 chr12: 46,167,102-46,178,403 ARID2
    nsv6937508copy number variation1nstd229human GRCh38 chr12: 45,817,526-45,817,586 , GRCh37.p13 chr12: 46,211,309-46,211,369 ARID2
    nsv6936805copy number variation1nstd229human GRCh38 chr12: 45,864,255-45,877,617 , GRCh37.p13 chr12: 46,258,038-46,271,400 RN7SL246P, ARID2
    nsv6935897copy number variation1nstd229human GRCh38 chr12: 45,842,005-45,843,286 , GRCh37.p13 chr12: 46,235,788-46,237,069 LOC105369745, ARID2
    nsv6933899copy number variation1nstd229human GRCh38 chr12: 45,855,012-45,855,181 , GRCh37.p13 chr12: 46,248,795-46,248,964 ARID2
    nsv6932632copy number variation1nstd229human GRCh38 chr12: 45,895,864-45,900,471 , GRCh37.p13 chr12: 46,289,647-46,294,254 ARID2
    nsv6932402copy number variation1nstd229human GRCh38 chr12: 45,745,101-45,747,400 , GRCh37.p13 chr12: 46,138,884-46,141,183 ARID2
    nsv6932167copy number variation1nstd229human GRCh38 chr12: 45,744,930-45,749,173 , GRCh37.p13 chr12: 46,138,713-46,142,956 ARID2
    nsv6932014copy number variation1nstd229human GRCh38 chr12: 45,782,505-45,785,458 , GRCh37.p13 chr12: 46,176,288-46,179,241 ARID2
    nsv6931825copy number variation1nstd229human GRCh38 chr12: 45,877,168-45,890,163 , GRCh37.p13 chr12: 46,270,951-46,283,946 ARID2, KNOP1P2
    nsv6929356copy number variation1nstd229human GRCh38 chr12: 45,886,151-45,886,189 , GRCh37.p13 chr12: 46,279,934-46,279,972 ARID2
    nsv6928544copy number variation1nstd229human GRCh38 chr12: 45,740,304-45,740,519 , GRCh37.p13 chr12: 46,134,087-46,134,302 ARID2
    nsv6922983copy number variation1nstd229human GRCh38 chr12: 45,766,848-45,766,926 , GRCh37.p13 chr12: 46,160,631-46,160,709 ARID2
    nsv6922869copy number variation1nstd229human GRCh38 chr12: 45,895,701-45,898,000 , GRCh37.p13 chr12: 46,289,484-46,291,783 ARID2
    nsv6921383copy number variation1nstd229human GRCh38 chr12: 45,732,478-45,737,783 , GRCh37.p13 chr12: 46,126,261-46,131,566 ARID2
    nsv6920793copy number variation1nstd229human GRCh38 chr12: 45,716,301-45,844,500 , GRCh37.p13 chr12: 46,110,084-46,238,283 LOC105369745, LINC00938, 1 more genes
    nsv6919059copy number variation1nstd229human GRCh38 chr12: 45,819,004-45,819,650 , GRCh37.p13 chr12: 46,212,787-46,213,433 ARID2
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