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Items: 1 to 20 of 331

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3885593copy number variation1nstd102humanBenign GRCh37 chr4: 70,350,444-70,353,585 , GRCh38.p12 chr4: 69,484,726-69,487,867 UGT2B4
    nsv6744065copy number variation1nstd229human GRCh38 chr4: 69,492,230-69,501,225 , GRCh37.p13 chr4: 70,357,948-70,366,943 UGT2B4
    nsv6756346copy number variation1nstd229human GRCh38 chr4: 69,506,599-69,515,120 , GRCh37.p13 chr4: 70,372,317-70,380,838 UGT2B4
    nsv6750097copy number variation1nstd229human GRCh38 chr4: 69,488,266-69,491,385 , GRCh37.p13 chr4: 70,353,984-70,357,103 UGT2B4
    nsv6378573copy number variation1nstd223human GRCh38 chr4: 69,494,101-69,495,100 , GRCh37.p13 chr4: 70,359,819-70,360,818 UGT2B4
    nsv6379633copy number variation1nstd223human GRCh38 chr4: 69,483,001-69,483,900 , GRCh37.p13 chr4: 70,348,719-70,349,618 UGT2B4
    nsv6385337copy number variation1nstd223human GRCh38 chr4: 69,503,272-69,504,159 , GRCh37.p13 chr4: 70,368,990-70,369,877 UGT2B4
    nsv6390239copy number variation1nstd223human GRCh38 chr4: 69,492,810-69,493,380 , GRCh37.p13 chr4: 70,358,528-70,359,098 UGT2B4
    nsv5469808copy number variation1nstd206human GRCh38 chr4: 69,492,205-69,501,244 , GRCh37.p13 chr4: 70,357,923-70,366,962 UGT2B4
    nsv5456508copy number variation1nstd206human GRCh38 chr4: 69,523,198-69,524,522 , GRCh37.p13 chr4: 70,388,916-70,390,240 UGT2B4
    nsv5463552copy number variation1nstd206human GRCh38 chr4: 69,506,589-69,506,704 , GRCh37.p13 chr4: 70,372,307-70,372,422 UGT2B4
    nsv5466895copy number variation1nstd206human GRCh38 chr4: 69,526,081-69,526,171 , GRCh37.p13 chr4: 70,391,799-70,391,889 UGT2B4
    nsv4659750copy number variation1nstd186human GRCh37 chr4: 70,388,911-70,390,240 , GRCh38.p12 chr4: 69,523,193-69,524,522 UGT2B4
    nsv6296896copy number variation1nstd186human GRCh37 chr4: 70,372,307-70,372,422 , GRCh38.p12 chr4: 69,506,589-69,506,704 UGT2B4
    nsv5998053copy number variation1nstd212human GRCh38 chr4: 69,523,197-69,524,527 , GRCh37.p13 chr4: 70,388,915-70,390,245 UGT2B4
    nsv4740198copy number variation1nstd199human GRCh37 chr4: 70,388,913-70,390,242 , GRCh38.p12 chr4: 69,523,195-69,524,524 UGT2B4
    nsv5318402copy number variation1nstd204human GRCh38.p13 chr4: 69,506,565-69,506,727 , GRCh37.p13 chr4: 70,372,283-70,372,445 UGT2B4
    nsv5901983copy number variation1nstd209human GRCh38 chr4: 69,523,193-69,524,521 , GRCh37.p13 chr4: 70,388,911-70,390,239 UGT2B4
    nsv4800117copy number variation1nstd200human GRCh37 chr4: 70,388,916-70,390,239 , GRCh38.p12 chr4: 69,523,198-69,524,521 UGT2B4
    nsv5905156copy number variation1nstd209human GRCh38 chr4: 69,506,587-69,506,703 , GRCh37.p13 chr4: 70,372,305-70,372,421 UGT2B4
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