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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5962263insertion1nstd209human GRCh38 chr2: 181,016,003-181,016,003 , GRCh37.p13 chr2: 181,880,730-181,880,730 UBE2E3
    nsv5952610insertion1nstd209human GRCh38 chr2: 181,041,232-181,041,232 , GRCh37.p13 chr2: 181,905,959-181,905,959 UBE2E3
    nsv5887679copy number variation1nstd209human GRCh38 chr2: 181,061,100-181,061,421 , GRCh37.p13 chr2: 181,925,827-181,926,148 UBE2E3
    nsv5681362mobile element insertion2nstd211human GRCh38 chr2: 181,016,019-181,016,019 , GRCh37.p13 chr2: 181,880,746-181,880,746 UBE2E3
    nsv5677298mobile element insertion1nstd211human GRCh38 chr2: 181,045,577-181,045,577 , GRCh37.p13 chr2: 181,910,304-181,910,304 UBE2E3
    nsv5621498insertion1nstd207human GRCh38 chr2: 181,021,578-181,021,578 , GRCh37.p13 chr2: 181,886,305-181,886,305 UBE2E3
    nsv5619204insertion1nstd207human GRCh38 chr2: 181,016,003-181,016,003 , GRCh37.p13 chr2: 181,880,730-181,880,730 UBE2E3
    nsv5617609insertion1nstd207human GRCh38 chr2: 181,021,554-181,021,554 , GRCh37.p13 chr2: 181,886,281-181,886,281 UBE2E3
    nsv5607045insertion1nstd207human GRCh38 chr2: 181,021,343-181,021,343 , GRCh37.p13 chr2: 181,886,070-181,886,070 UBE2E3
    nsv5605054insertion2nstd207human GRCh38 chr2: 181,021,562-181,021,562 , GRCh37.p13 chr2: 181,886,289-181,886,289 UBE2E3
    nsv5564646copy number variation1nstd207human GRCh38 chr2: 181,061,100-181,061,421 , GRCh37.p13 chr2: 181,925,827-181,926,148 UBE2E3
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5452476copy number variation1nstd206human GRCh38 chr2: 181,061,110-181,061,422 , GRCh37.p13 chr2: 181,925,837-181,926,149 UBE2E3
    nsv5441326copy number variation1nstd206human GRCh38 chr2: 181,033,791-181,034,132 , GRCh37.p13 chr2: 181,898,518-181,898,859 UBE2E3
    nsv5406544mobile element insertion1nstd206human GRCh38 chr2: 181,016,003-181,016,003 , GRCh37.p13 chr2: 181,880,730-181,880,730 UBE2E3
    nsv5399879mobile element insertion1nstd206human GRCh38 chr2: 181,045,577-181,045,628 , GRCh37.p13 chr2: 181,910,304-181,910,355 UBE2E3
    nsv5382100mobile element deletion2nstd186human GRCh37 chr2: 181,925,837-181,926,149 , GRCh38.p12 chr2: 181,061,110-181,061,422 UBE2E3
    nsv5381341copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,999,572-182,774,361 , GRCh38.p12 chr2: 171,143,062-181,909,634 ALDH7A1P2, LOC101927055, 174 more genes
    nsv5351050translocation1nstd200human GRCh38 chr2: 181,048,590-181,048,590 , GRCh38 chr2: 181,049,901-181,049,901 , GRCh37.p13 chr2: 181,913,317-181,913,317 , GRCh37.p13 chr2: 181,914,628-181,914,628 UBE2E3
    nsv5351049translocation1nstd200human GRCh38 chr2: 181,036,953-181,036,953 , GRCh38 chr2: 181,037,056-181,037,056 , GRCh37.p13 chr2: 181,901,680-181,901,680 , GRCh37.p13 chr2: 181,901,783-181,901,783 UBE2E3
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