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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5720757mobile element insertion1nstd211human GRCh38 chr2: 233,770,878-233,770,878 , GRCh37.p13 chr2: 234,679,524-234,679,524 UGT1A8, UGT1A3, 8 more genes
    nsv5687108mobile element insertion1nstd211human GRCh38 chr2: 233,767,249-233,767,249 , GRCh37.p13 chr2: 234,675,895-234,675,895 UGT1A10, UGT1A3, 8 more genes
    nsv5566372copy number variation1nstd207human GRCh38 chr2: 233,762,426-233,763,135 , GRCh37.p13 chr2: 234,671,072-234,671,781 UGT1A3, UGT1A5, 8 more genes
    nsv5558450mobile element insertion1nstd206human GRCh38 chr2: 233,770,878-233,770,929 , GRCh37.p13 chr2: 234,679,524-234,679,575 UGT1A10, UGT1A6, 8 more genes
    nsv5443355copy number variation1nstd206human GRCh38 chr2: 233,762,430-233,763,136 , GRCh37.p13 chr2: 234,671,076-234,671,782 UGT1A, UGT1A7, 8 more genes
    nsv5403788mobile element insertion1nstd206human GRCh38 chr2: 233,767,249-233,767,300 , GRCh37.p13 chr2: 234,675,895-234,675,946 UGT1A1, UGT1A7, 8 more genes
    nsv5312665copy number variation1nstd204human GRCh38.p13 chr2: 233,762,408-233,763,157 , GRCh37.p13 chr2: 234,671,054-234,671,803 UGT1A9, UGT1A, 8 more genes
    nsv4926766copy number variation1nstd200human GRCh38 chr2: 233,762,430-233,763,136 , GRCh37.p13 chr2: 234,671,076-234,671,782 UGT1A9, UGT1A, 8 more genes
    nsv4806335copy number variation1nstd200human GRCh37 chr2: 234,671,076-234,671,782 , GRCh38.p12 chr2: 233,762,430-233,763,136 UGT1A, UGT1A10, 8 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4674274copy number variation1nstd102humanPathogenic GRCh37 chr2: 234,090,049-239,494,702 , GRCh38.p12 chr2: 233,181,403-238,586,061 LOC105373933, CEP19P1, 105 more genes
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4466653mobile element insertion1nstd166human GRCh37.p13 chr2: 234,674,809-234,674,809 , GRCh38.p12 chr2: 233,766,163-233,766,163 UGT1A4, UGT1A3, 8 more genes
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 XRCC5, LINC01173, 494 more genes
    nsv4387396copy number variation1nstd173human GRCh37 chr2: 234,613,007-234,699,819 , GRCh38.p12 chr2: 233,704,361-233,791,173 UGT1A6, UGT1A1, 13 more genes
    nsv4370732copy number variation1nstd173human GRCh37 chr2: 234,609,804-234,699,819 , GRCh38.p12 chr2: 233,701,158-233,791,173 RPL17P11, UGT1A5, 13 more genes
    nsv4366560copy number variation2nstd173human GRCh37 chr2: 234,613,019-234,699,807 , GRCh38.p12 chr2: 233,704,373-233,791,161 UGT1A, UGT1A9, 13 more genes
    nsv4333696sequence alteration1nstd166human GRCh37.p13 chr2: 234,681,475-234,695,009 , GRCh38.p12 chr2: 233,772,829-233,786,363 UGT1A9, UGT1A1, 9 more genes
    nsv4082673copy number variation1nstd166human GRCh37.p13 chr2: 234,552,582-235,494,274 , GRCh38.p12 chr2: 233,643,936-234,585,630 LOC105373933, UGT1A6, 24 more genes
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