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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5722779mobile element insertion1nstd211human GRCh38 chr12: 69,354,195-69,354,195 , GRCh37.p13 chr12: 69,747,975-69,747,975 LYZ
    nsv5556951sequence alteration1nstd206human GRCh38 chr12: 68,612,001-69,442,414 , GRCh37.p13 chr12: 69,005,781-69,836,194 , LYZ, 22 more genes
    nsv5502346copy number variation1nstd206human GRCh38 chr12: 69,353,735-69,363,240 , GRCh37.p13 chr12: 69,747,515-69,757,020 YEATS4, LYZ
    nsv5194428mobile element insertion1nstd203human GRCh38 chr12: 69,348,257-69,348,257 , GRCh37.p13 chr12: 69,742,037-69,742,037 LYZ
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    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
    nsv4729265copy number variation1nstd102humanPathogenic GRCh37 chr12: 68,572,386-70,833,868 , GRCh38.p12 chr12: 68,178,606-70,440,088 LINC02384, LOC101928002, 47 more genes
    nsv4681833copy number variation1nstd102humanUncertain significance GRCh37 chr12: 69,742,189-69,746,999 , GRCh38.p12 chr12: 69,348,409-69,353,219 LYZ
    nsv4574984mobile element insertion1nstd166human GRCh37.p13 chr12: 69,742,025-69,742,025 , GRCh38.p12 chr12: 69,348,245-69,348,245 LYZ
    nsv4557437sequence alteration1nstd166human GRCh38.p12 chr12: 69,346,962-69,514,777 , GRCh37.p13 chr12: 69,740,742-69,908,557 LYZ, YEATS4, 5 more genes
    nsv4345788sequence alteration1nstd166human GRCh37.p13 chr12: 59,785,153-101,478,055 , GRCh38.p12 chr12: 59,391,372-101,084,277 , APAF1, 538 more genes
    nsv4340108sequence alteration1nstd166human GRCh37.p13 chr12: 69,005,781-69,836,194 , GRCh38.p12 chr12: 68,612,001-69,442,414 , RAP1B, 22 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv4205588copy number variation1nstd166human GRCh37.p13 chr12: 69,747,486-69,757,072 , GRCh38.p12 chr12: 69,353,706-69,363,292 LYZ, YEATS4
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