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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6936854copy number variation1nstd229human GRCh38 chr12: 85,805,301-85,879,881 , GRCh37.p13 chr12: 86,199,079-86,273,659 NTS, RASSF9
    nsv6934024copy number variation1nstd229human GRCh38 chr12: 85,872,571-85,876,038 , GRCh37.p13 chr12: 86,266,349-86,269,816 NTS
    nsv6927797copy number variation1nstd229human GRCh38 chr12: 85,871,876-85,875,756 , GRCh37.p13 chr12: 86,265,654-86,269,534 NTS
    nsv6926811copy number variation1nstd229human GRCh38 chr12: 85,877,738-85,907,973 , GRCh37.p13 chr12: 86,271,516-86,301,751 NTS
    nsv6923854copy number variation1nstd229human GRCh38 chr12: 85,545,377-85,901,300 , GRCh37.p13 chr12: 85,939,155-86,295,078 LOC101059974, LOC100129589, 3 more genes
    nsv6923827copy number variation1nstd229human GRCh38 chr12: 85,678,894-86,195,253 , GRCh37.p13 chr12: 86,072,672-86,589,031 NTS, RASSF9, 2 more genes
    nsv6920168copy number variation1nstd229human GRCh38 chr12: 85,881,847-85,956,435 , GRCh37.p13 chr12: 86,275,625-86,350,214 NTS, MGAT4C
    nsv6635723copy number variation1nstd227human GRCh38.p12 chr12: 85,881,965-85,918,073 , GRCh37 chr12: 86,275,743-86,311,851 NTS
    nsv6621757copy number variation1nstd224human GRCh37 chr12: 85,957,254-86,280,867 , GRCh38.p12 chr12: 85,563,476-85,887,089 RASSF9, NTS, 3 more genes
    nsv6621626copy number variation2nstd224human GRCh37 chr12: 85,942,397-86,293,214 , GRCh38.p12 chr12: 85,548,619-85,899,436 LOC101059974, RASSF9, 3 more genes
    nsv6465202copy number variation1nstd223human GRCh38 chr12: 85,805,301-85,879,875 , GRCh37.p13 chr12: 86,199,079-86,273,653 RASSF9, NTS
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132717copy number variation1nstd213human GRCh37 chr12: 86,270,000-86,640,001 , GRCh38.p12 chr12: 85,876,222-86,246,223 NTS, MGAT4C
    nsv6132715copy number variation1nstd213human GRCh37 chr12: 84,440,000-93,800,001 , GRCh38.p12 chr12: 84,046,221-93,406,225 , BTG1, 102 more genes
    nsv6132617copy number variation1nstd213human GRCh37 chr12: 85,560,000-86,500,001 , GRCh38.p12 chr12: 85,166,222-86,106,223 NTS, ALX1, 7 more genes
    nsv6099373insertion1nstd212human GRCh38 chr12: 85,879,168-85,879,168 , GRCh37.p13 chr12: 86,272,946-86,272,946 NTS
    nsv6095354insertion1nstd212human GRCh38 chr12: 85,879,786-85,879,786 , GRCh37.p13 chr12: 86,273,564-86,273,564 NTS
    nsv6090300insertion1nstd212human GRCh38 chr12: 85,879,589-85,879,589 , GRCh37.p13 chr12: 86,273,367-86,273,367 NTS
    nsv5928971copy number variation1nstd209human GRCh38 chr12: 85,879,206-85,879,391 , GRCh37.p13 chr12: 86,272,984-86,273,169 NTS
    nsv5661191insertion1nstd207human GRCh38 chr12: 85,879,264-85,879,264 , GRCh37.p13 chr12: 86,273,042-86,273,042 NTS
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