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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148098copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 121,890,923-122,473,333 , GRCh38.p12 chr12: 121,453,120-122,035,427 BCL7A, HPD, 14 more genes
    nsv7148095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,341,598-124,103,434 , GRCh38.p12 chr12: 120,903,795-123,618,887 ANAPC5, MLXIP, 82 more genes
    nsv6934866copy number variation1nstd229human GRCh38 chr12: 119,918,701-123,974,100 , GRCh37.p13 chr12: 120,356,505-124,458,647 RNU6-1088P, LOC105370042, 130 more genes
    nsv6932114copy number variation1nstd229human GRCh38 chr12: 121,812,438-121,812,468 , GRCh37.p13 chr12: 122,250,344-122,250,374 SETD1B
    nsv6931724copy number variation1nstd229human GRCh38 chr12: 121,803,601-121,805,700 , GRCh37.p13 chr12: 122,241,507-122,243,606 SETD1B
    nsv6930503copy number variation1nstd229human GRCh38 chr12: 121,793,001-121,805,800 , GRCh37.p13 chr12: 122,230,907-122,243,706 SETD1B, LINC01089, 1 more genes
    nsv6920920copy number variation1nstd229human GRCh38 chr12: 121,001,001-122,266,400 , GRCh37.p13 chr12: 121,438,804-122,750,947 BCL7A, KDM2B, 36 more genes
    nsv6583876inversion1nstd223human GRCh38 chr12: 118,054,469-123,705,974 , GRCh37.p13 chr12: 118,492,274-124,190,521 RPL11P5, RPL17P37, 159 more genes
    nsv6291677copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,970,346-122,287,290 , GRCh38.p12 chr12: 121,532,441-121,849,384 KDM2B, ORAI1, 9 more genes
    nsv6290266copy number variation1nstd102humanUncertain significance GRCh37 chr12: 121,887,337-123,386,068 , GRCh38.p12 chr12: 121,449,534-122,901,521 LINC02985, DENR, 38 more genes
    nsv6290239copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 117,461,902-133,841,395 , GRCh38.p12 chr12: 117,024,097-133,264,809 ACADS, BCL7A, 356 more genes
    nsv6248658mobile element insertion1nstd215human GRCh38 chr12: 121,811,282-121,811,282 , GRCh37.p13 chr12: 122,249,188-122,249,188 SETD1B
    nsv6132413copy number variation1nstd213human GRCh37 chr12: 121,590,000-123,620,001 , GRCh38.p12 chr12: 121,152,197-123,135,454 BCL7A, HPD, 51 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5494852copy number variation1nstd206human GRCh38 chr12: 121,806,730-121,806,806 , GRCh37.p13 chr12: 122,244,636-122,244,712 SETD1B
    nsv5356465translocation1nstd200human GRCh38 chr12: 121,822,952-121,822,952 , GRCh38 chr12: 121,822,891-121,822,891 , GRCh37.p13 chr12: 122,260,797-122,260,797 , GRCh37.p13 chr12: 122,260,858-122,260,858 SETD1B
    nsv5331502translocation1nstd200human GRCh37 chr12: 122,244,636-122,244,636 , GRCh37 chr12: 122,244,712-122,244,712 , GRCh38.p12 chr12: 121,806,806-121,806,806 , GRCh38.p12 chr12: 121,806,730-121,806,730 SETD1B
    nsv5262460copy number variation1nstd204human GRCh38.p13 chr12: 121,802,216-121,803,265 , GRCh37.p13 chr12: 122,240,122-122,241,171 SETD1B, LINC01089
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
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