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Items: 1 to 20 of 273

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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
    nsv6776854copy number variation1nstd229human GRCh38 chr5: 38,850,953-38,851,152 , GRCh37.p13 chr5: 38,851,055-38,851,254 OSMR
    nsv6776658copy number variation1nstd229human GRCh38 chr5: 38,895,983-38,896,986 , GRCh37.p13 chr5: 38,896,085-38,897,088 OSMR
    nsv6772998copy number variation1nstd229human GRCh38 chr5: 38,902,666-38,905,340 , GRCh37.p13 chr5: 38,902,768-38,905,442 OSMR
    nsv6772345copy number variation1nstd229human GRCh38 chr5: 38,875,682-38,878,496 , GRCh37.p13 chr5: 38,875,784-38,878,598 OSMR
    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
    nsv6767707copy number variation1nstd229human GRCh38 chr5: 38,854,954-38,857,634 , GRCh37.p13 chr5: 38,855,056-38,857,736 OSMR
    nsv6765022copy number variation1nstd229human GRCh38 chr5: 38,902,665-38,905,343 , GRCh37.p13 chr5: 38,902,767-38,905,445 OSMR
    nsv6764301copy number variation1nstd229human GRCh38 chr5: 37,395,324-40,706,253 , GRCh37.p13 chr5: 37,395,426-40,706,355 DAB2, LOC107986414, 39 more genes
    nsv6763141copy number variation1nstd229human GRCh38 chr5: 38,928,724-38,930,989 , GRCh37.p13 chr5: 38,928,826-38,931,091 OSMR
    nsv6760118copy number variation1nstd229human GRCh38 chr5: 38,835,313-38,848,898 , GRCh37.p13 chr5: 38,835,415-38,849,000 OSMR, OSMR-DT
    nsv6759520copy number variation1nstd229human GRCh38 chr5: 38,855,001-38,857,600 , GRCh37.p13 chr5: 38,855,103-38,857,702 OSMR
    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
    nsv6636941copy number variation1nstd102humanUncertain significance GRCh37 chr5: 38,747,296-39,159,120 , GRCh38.p12 chr5: 38,747,194-39,159,018 RICTOR, AIG1P1, 5 more genes
    nsv6561104inversion1nstd223human GRCh38 chr5: 38,861,070-38,876,646 , GRCh37.p13 chr5: 38,861,172-38,876,748 OSMR
    nsv6394574copy number variation1nstd223human GRCh38 chr5: 38,907,101-38,908,800 , GRCh37.p13 chr5: 38,907,203-38,908,902 OSMR
    nsv6392293copy number variation1nstd223human GRCh38 chr5: 38,841,601-38,865,000 , GRCh37.p13 chr5: 38,841,703-38,865,102 OSMR-DT, OSMR
    nsv6390852copy number variation1nstd223human GRCh38 chr5: 38,937,901-38,940,000 , GRCh37.p13 chr5: 38,938,003-38,940,102 RICTOR, OSMR
    nsv6386722copy number variation1nstd223human GRCh38 chr5: 38,858,501-38,860,400 , GRCh37.p13 chr5: 38,858,603-38,860,502 OSMR
    nsv6385083copy number variation1nstd223human GRCh38 chr5: 38,895,987-38,896,986 , GRCh37.p13 chr5: 38,896,089-38,897,088 OSMR
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