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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052644inversion1nstd229human GRCh38 chr4: 69,587,673-69,600,012 , GRCh37.p13 chr4: 70,453,391-70,465,730 UGT2A2, UGT2A1
    nsv7042173inversion1nstd229human GRCh38 chr4: 69,616,175-69,640,179 , GRCh37.p13 chr4: 70,481,893-70,505,897 UGT2A1, UGT2A2
    nsv7041783inversion1nstd229human GRCh38 chr4: 69,619,394-69,621,522 , GRCh37.p13 chr4: 70,485,112-70,487,240 UGT2A2, UGT2A1
    nsv7041094inversion1nstd229human GRCh38 chr4: 69,587,211-69,631,314 , GRCh37.p13 chr4: 70,452,929-70,497,032 UGT2A2, UGT2A1
    nsv6757416copy number variation1nstd229human GRCh38 chr4: 68,526,545-69,660,672 , GRCh37.p13 chr4: 69,392,263-70,526,390 UGT2B26P, UGT2B11, 37 more genes
    nsv6757299copy number variation1nstd229human GRCh38 chr4: 69,570,044-69,595,503 , GRCh37.p13 chr4: 70,435,762-70,461,221 LOC100422024, UGT2A1, 1 more genes
    nsv6755453copy number variation1nstd229human GRCh38 chr4: 68,793,720-69,854,262 , GRCh37.p13 chr4: 69,659,438-70,719,980 SPOPLP1, UGT2B4, 33 more genes
    nsv6752371copy number variation1nstd229human GRCh38 chr4: 69,601,501-69,608,300 , GRCh37.p13 chr4: 70,467,219-70,474,018 UGT2A1, UGT2A2
    nsv6752258copy number variation1nstd229human GRCh38 chr4: 69,600,001-69,631,300 , GRCh37.p13 chr4: 70,465,719-70,497,018 UGT2A1, UGT2A2
    nsv6749958copy number variation1nstd229human GRCh38 chr4: 69,603,201-69,608,400 , GRCh37.p13 chr4: 70,468,919-70,474,118 UGT2A2, UGT2A1
    nsv6749752copy number variation1nstd229human GRCh38 chr4: 68,786,846-69,797,610 , GRCh37.p13 chr4: 69,652,564-70,663,328 UGT2A2, UGT2B10, 33 more genes
    nsv6749461copy number variation1nstd229human GRCh38 chr4: 69,602,401-69,610,900 , GRCh37.p13 chr4: 70,468,119-70,476,618 UGT2A1, UGT2A2
    nsv6746769copy number variation1nstd229human GRCh38 chr4: 69,087,431-73,565,096 , GRCh37.p13 chr4: 69,953,149-74,430,813 LOC642496, CSN2, 76 more genes
    nsv6746645copy number variation1nstd229human GRCh38 chr4: 69,601,739-69,607,094 , GRCh37.p13 chr4: 70,467,457-70,472,812 UGT2A1, UGT2A2
    nsv6745554copy number variation1nstd229human GRCh38 chr4: 69,589,894-69,643,023 , GRCh37.p13 chr4: 70,455,612-70,508,741 UGT2A2, UGT2A1
    nsv6744637copy number variation1nstd229human GRCh38 chr4: 69,558,322-69,658,750 , GRCh37.p13 chr4: 70,424,040-70,524,468 LOC100422024, UGT2A2, 1 more genes
    nsv6743934copy number variation1nstd229human GRCh38 chr4: 69,613,792-69,624,081 , GRCh37.p13 chr4: 70,479,510-70,489,799 UGT2A2, UGT2A1
    nsv6741395copy number variation1nstd229human GRCh38 chr4: 69,621,540-69,651,109 , GRCh37.p13 chr4: 70,487,258-70,516,827 UGT2A2, UGT2A1
    nsv6740438copy number variation1nstd229human GRCh38 chr4: 69,593,301-69,611,100 , GRCh37.p13 chr4: 70,459,019-70,476,818 UGT2A2, UGT2A1
    nsv6636838copy number variation1nstd102humanUncertain significance GRCh37 chr4: 70,479,061-70,985,189 , GRCh38.p12 chr4: 69,613,343-70,119,472 HTN3, LOC105377269, 10 more genes
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