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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
    nsv5927946copy number variation1nstd209human GRCh38 chr12: 72,261,882-72,263,410 , GRCh37.p13 chr12: 72,655,662-72,657,190 TRHDE-AS1, TRHDE
    nsv5713751mobile element insertion1nstd211human GRCh38 chr12: 72,267,597-72,267,597 , GRCh37.p13 chr12: 72,661,377-72,661,377 TRHDE-AS1, TRHDE
    nsv5508415copy number variation1nstd206human GRCh38 chr12: 72,261,882-72,263,411 , GRCh37.p13 chr12: 72,655,662-72,657,191 TRHDE, TRHDE-AS1
    nsv5430878mobile element insertion1nstd206human GRCh38 chr12: 72,267,597-72,267,648 , GRCh37.p13 chr12: 72,661,377-72,661,428 TRHDE-AS1, TRHDE
    nsv5132831mobile element insertion1nstd203human GRCh38 chr12: 72,267,584-72,267,594 , GRCh37.p13 chr12: 72,661,364-72,661,374 TRHDE-AS1, TRHDE
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 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
    nsv5005963copy number variation1nstd200human GRCh38 chr12: 72,261,882-72,263,411 , GRCh37.p13 chr12: 72,655,662-72,657,191 TRHDE-AS1, TRHDE
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 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
    nsv4667788copy number variation1nstd186human GRCh37 chr12: 72,655,662-72,657,191 , GRCh38.p12 chr12: 72,261,882-72,263,411 TRHDE-AS1, TRHDE
    nsv4609536copy number variation1nstd183human GRCh37 chr12: 72,655,662-72,657,191 , GRCh38.p12 chr12: 72,261,882-72,263,411 TRHDE, TRHDE-AS1
    nsv4562899mobile element insertion1nstd166human GRCh37.p13 chr12: 72,658,268-72,658,268 , GRCh38.p12 chr12: 72,264,488-72,264,488 TRHDE, TRHDE-AS1
    nsv4516031mobile element insertion1nstd166human GRCh37.p13 chr12: 72,651,460-72,651,460 , GRCh38.p12 chr12: 72,257,680-72,257,680 TRHDE, TRHDE-AS1
    nsv4513266mobile element insertion1nstd166human GRCh37.p13 chr12: 72,661,364-72,661,364 , GRCh38.p12 chr12: 72,267,584-72,267,584 TRHDE, TRHDE-AS1
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