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Items: 1 to 20 of 472

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071639inversion1nstd229human GRCh38 chr15: 57,688,637-57,688,695 , GRCh37.p13 chr15: 57,980,835-57,980,893 GCOM1
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv7069841inversion1nstd229human GRCh38 chr15: 55,108,583-62,405,114 , GRCh37.p13 chr15: 55,400,781-62,697,313 LOC105370834, RPL21P14, 118 more genes
    nsv6971873copy number variation1nstd229human GRCh38 chr15: 57,651,499-57,679,100 , GRCh37.p13 chr15: 57,943,697-57,971,298 MYZAP, GCOM1
    nsv6971755copy number variation1nstd229human GRCh38 chr15: 57,673,933-57,674,036 , GRCh37.p13 chr15: 57,966,131-57,966,234 GCOM1, MYZAP
    nsv6970023copy number variation1nstd229human GRCh38 chr15: 57,569,774-57,626,699 , GRCh37.p13 chr15: 57,861,972-57,918,897 GCOM1, MYZAP
    nsv6969603copy number variation1nstd229human GRCh38 chr15: 57,661,534-57,684,480 , GRCh37.p13 chr15: 57,953,732-57,976,678 MYZAP, GCOM1
    nsv6969056copy number variation1nstd229human GRCh38 chr15: 57,581,285-57,611,667 , GRCh37.p13 chr15: 57,873,483-57,903,865 GCOM1, MYZAP
    nsv6968721copy number variation1nstd229human GRCh38 chr15: 57,622,414-57,625,419 , GRCh37.p13 chr15: 57,914,612-57,917,617 GCOM1, MYZAP
    nsv6964322copy number variation1nstd229human GRCh38 chr15: 57,675,068-57,684,398 , GRCh37.p13 chr15: 57,967,266-57,976,596 MYZAP, GCOM1
    nsv6963338copy number variation1nstd229human GRCh38 chr15: 57,717,901-57,729,400 , GRCh37.p13 chr15: 58,010,099-58,021,598 GCOM1, POLR2M
    nsv6963332copy number variation1nstd229human GRCh38 chr15: 57,526,009-57,699,984 , GRCh37.p13 chr15: 57,818,207-57,992,182 RPS13P7, CGNL1, 2 more genes
    nsv6960662copy number variation1nstd229human GRCh38 chr15: 57,587,413-57,617,922 , GRCh37.p13 chr15: 57,879,611-57,910,120 MYZAP, GCOM1
    nsv6959734copy number variation1nstd229human GRCh38 chr15: 57,704,445-57,705,070 , GRCh37.p13 chr15: 57,996,643-57,997,268 GCOM1, POLR2M
    nsv6959354copy number variation1nstd229human GRCh38 chr15: 57,696,551-57,696,915 , GRCh37.p13 chr15: 57,988,749-57,989,113 GCOM1
    nsv6959286copy number variation1nstd229human GRCh38 chr15: 57,704,575-57,705,071 , GRCh37.p13 chr15: 57,996,773-57,997,269 GCOM1, POLR2M
    nsv6958808copy number variation1nstd229human GRCh38 chr15: 57,666,212-57,668,196 , GRCh37.p13 chr15: 57,958,410-57,960,394 GCOM1, MYZAP
    nsv6958654copy number variation1nstd229human GRCh38 chr15: 57,655,401-57,663,400 , GRCh37.p13 chr15: 57,947,599-57,955,598 MYZAP, GCOM1
    nsv6958488copy number variation1nstd229human GRCh38 chr15: 57,692,633-57,693,595 , GRCh37.p13 chr15: 57,984,831-57,985,793 GCOM1
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
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