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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7057133inversion1nstd229human GRCh38 chr5: 35,951,379-35,951,394 , GRCh37.p13 chr5: 35,951,481-35,951,496 UGT3A1
    nsv7048789inversion1nstd229human GRCh38 chr5: 35,602,363-36,053,738 , GRCh37.p13 chr5: 35,602,465-36,053,840 UGT3A1, RNU7-130P, 6 more genes
    nsv6777774copy number variation1nstd229human GRCh38 chr5: 35,947,573-35,950,041 , GRCh37.p13 chr5: 35,947,675-35,950,143 UGT3A1
    nsv6775022copy number variation1nstd229human GRCh38 chr5: 35,987,410-35,995,410 , GRCh37.p13 chr5: 35,987,512-35,995,512 UGT3A1
    nsv6774881copy number variation1nstd229human GRCh38 chr5: 35,999,996-36,005,317 , GRCh37.p13 chr5: 36,000,098-36,005,419 UGT3A1
    nsv6769429copy number variation1nstd229human GRCh38 chr5: 35,077,787-40,637,192 , GRCh37.p13 chr5: 35,077,889-40,637,294 LINC02110, LOC105374735, 68 more genes
    nsv6769154copy number variation1nstd229human GRCh38 chr5: 35,947,342-35,952,077 , GRCh37.p13 chr5: 35,947,444-35,952,179 UGT3A1
    nsv6767469copy number variation1nstd229human GRCh38 chr5: 35,976,321-35,981,753 , GRCh37.p13 chr5: 35,976,423-35,981,855 UGT3A1
    nsv6759649copy number variation1nstd229human GRCh38 chr5: 35,960,850-35,964,463 , GRCh37.p13 chr5: 35,960,952-35,964,565 UGT3A1
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6630342copy number variation1nstd224human GRCh37 chr5: 35,694,454-36,110,716 , GRCh38.p12 chr5: 35,694,352-36,110,614 IL7R, SPEF2, 6 more genes
    nsv6572148inversion1nstd223human GRCh38 chr5: 33,560,391-36,411,977 , GRCh37.p13 chr5: 33,560,496-36,412,079 C1QTNF3, RAI14-DT, 36 more genes
    nsv6556571inversion1nstd223human GRCh38 chr5: 35,979,202-35,981,802 , GRCh37.p13 chr5: 35,979,304-35,981,904 UGT3A1
    nsv6394842copy number variation1nstd223human GRCh38 chr5: 35,987,410-35,995,407 , GRCh37.p13 chr5: 35,987,512-35,995,509 UGT3A1
    nsv6394727copy number variation1nstd223human GRCh38 chr5: 36,000,013-36,001,945 , GRCh37.p13 chr5: 36,000,115-36,002,047 UGT3A1
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
    nsv6300383copy number variation1nstd186human GRCh37 chr5: 26,834,087-43,674,516 , GRCh38.p12 chr5: 26,833,978-43,674,414 , TMEM267, 221 more genes
    nsv6147985copy number variation1nstd214human GRCh38 chr5: 35,962,774-35,962,838 , GRCh37.p13 chr5: 35,962,876-35,962,940 UGT3A1
    nsv6135406copy number variation1nstd213human GRCh37 chr5: 31,280,000-36,080,001 , GRCh38.p12 chr5: 31,279,893-36,079,899 IL7R, NPR3, 64 more genes
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