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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074786inversion1nstd229human GRCh38 chr12: 47,059,202-48,408,098 , GRCh37.p13 chr12: 47,452,985-48,801,881 LOC102725258, RPAP3, 42 more genes
    nsv6923530copy number variation1nstd229human GRCh38 chr12: 48,154,586-48,248,092 , GRCh37.p13 chr12: 48,548,369-48,641,875 PHB1P18, OR10AD1, 5 more genes
    nsv6918615copy number variation1nstd229human GRCh38 chr12: 47,957,960-48,181,643 , GRCh37.p13 chr12: 48,351,743-48,575,426 PHB1P18, SENP1, 12 more genes
    nsv6637635copy number variation1nstd102humanUncertain significance GRCh37 chr12: 48,380,031-48,542,853 , GRCh38.p12 chr12: 47,986,248-48,149,070 LOC105369750, MIR6505, 7 more genes
    nsv6634445copy number variation1nstd102humanPathogenic GRCh37 chr12: 44,661,149-48,921,204 , GRCh38.p12 chr12: 44,267,366-48,527,421 ZNF641, MIR4698, 77 more genes
    nsv6132248copy number variation1nstd213human GRCh37 chr12: 45,960,000-49,240,001 , GRCh38.p12 chr12: 45,566,217-48,846,218 LALBA, VDR, 83 more genes
    nsv6039506copy number variation1nstd212human GRCh38 chr12: 48,155,811-48,155,878 , GRCh37.p13 chr12: 48,549,594-48,549,661 ASB8
    nsv5564512copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 37,873,948-49,578,619 , GRCh38.p12 chr12: 37,480,146-49,184,836 ADCY6, ABCD2, 187 more genes
    nsv5512307copy number variation1nstd206human GRCh38 chr12: 48,143,071-48,364,591 , GRCh37.p13 chr12: 48,536,854-48,758,374 LOC100533659, PHB1P18, 10 more genes
    nsv5508402copy number variation1nstd206human GRCh38 chr12: 48,156,419-48,156,469 , GRCh37.p13 chr12: 48,550,202-48,550,252 ASB8
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5029954inversion1nstd200human GRCh38 chr12: 38,328,571-48,487,625 , GRCh37.p13 chr12: 38,722,373-48,881,408 , MESDP1, 138 more genes
    nsv4972512copy number variation1nstd200human GRCh38 chr12: 48,155,108-48,155,757 , GRCh37.p13 chr12: 48,548,891-48,549,540 ASB8
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4731127copy number variation1nstd199human GRCh37 chr12: 48,549,597-48,549,664 , GRCh38.p12 chr12: 48,155,814-48,155,881 ASB8
    nsv4555165insertion1nstd166human GRCh37.p13 chr12: 48,549,504-48,549,504 , GRCh38.p12 chr12: 48,155,721-48,155,721 ASB8
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv3920847inversion1nstd102humanUncertain significance GRCh38.p12 chr12: 26,217,318-53,967,754 , GRCh37 chr12: 26,370,251-54,361,538 , ASIC1, 491 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
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