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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7094203copy number variation1nstd102humanUncertain significance GRCh37 chr12: 122,277,634-124,242,579 , GRCh38.p12 chr12: 121,839,728-123,758,032 SBNO1, MIR9902-1, 58 more genes
    nsv7071183inversion1nstd229human GRCh38 chr12: 122,804,561-124,735,813 , GRCh37.p13 chr12: 123,289,108-125,220,359 TMED2, GTF2H3, 41 more genes
    nsv7058574inversion1nstd229human GRCh38 chr12: 122,435,128-123,376,948 , GRCh37.p13 chr12: 122,919,675-123,861,495 RNA5SP375, HCAR1, 23 more genes
    nsv6935578copy number variation1nstd229human GRCh38 chr12: 122,801,773-122,849,881 , GRCh37.p13 chr12: 123,286,320-123,334,428 CCDC62, HIP1R
    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
    nsv6933168copy number variation1nstd229human GRCh38 chr12: 122,778,172-122,842,916 , GRCh37.p13 chr12: 123,262,719-123,327,463 CCDC62, HIP1R
    nsv6924408copy number variation1nstd229human GRCh38 chr12: 122,644,242-123,080,927 , GRCh37.p13 chr12: 123,128,789-123,565,474 VPS37B, MIR9902-1, 13 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
    nsv6495235copy number variation1nstd223human GRCh38 chr12: 122,582,127-122,928,683 , GRCh37.p13 chr12: 123,066,674-123,413,230 MIR9902-2, VPS37B, 9 more genes
    nsv6490069copy number variation1nstd223human GRCh38 chr12: 122,825,460-122,837,653 , GRCh37.p13 chr12: 123,310,007-123,322,200 CCDC62, HIP1R
    nsv6477465copy number variation1nstd223human GRCh38 chr12: 122,828,896-122,838,116 , GRCh37.p13 chr12: 123,313,443-123,322,663 HIP1R
    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
    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
    nsv6037784copy number variation1nstd212human GRCh38 chr12: 122,853,397-122,853,549 , GRCh37.p13 chr12: 123,337,944-123,338,096 HIP1R
    nsv6024471copy number variation1nstd212human GRCh38 chr12: 122,850,390-122,850,464 , GRCh37.p13 chr12: 123,334,937-123,335,011 HIP1R
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5595967copy number variation1nstd207human GRCh38 chr12: 122,853,216-122,853,339 , GRCh37.p13 chr12: 123,337,763-123,337,886 HIP1R
    nsv5594903copy number variation1nstd207human GRCh38 chr12: 122,850,507-122,850,567 , GRCh37.p13 chr12: 123,335,054-123,335,114 HIP1R
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