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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074787inversion1nstd229human GRCh38 chr15: 59,615,252-60,468,571 , GRCh37.p13 chr15: 59,907,451-60,760,770 BNIP2, ICE2, 14 more genes
    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
    nsv7059200inversion1nstd229human GRCh38 chr15: 59,449,988-59,734,427 , GRCh37.p13 chr15: 59,742,187-60,026,626 GTF2A2, PIGHP1, 6 more genes
    nsv6977337copy number variation1nstd229human GRCh38 chr15: 59,600,718-59,627,349 , GRCh37.p13 chr15: 59,892,917-59,919,548 GCNT3
    nsv6976334copy number variation1nstd229human GRCh38 chr15: 59,533,256-59,675,881 , GRCh37.p13 chr15: 59,825,455-59,968,080 BNIP2, GCNT3, 4 more genes
    nsv6974883copy number variation1nstd229human GRCh38 chr15: 59,607,334-59,651,116 , GRCh37.p13 chr15: 59,899,533-59,943,315 GTF2A2, GCNT3
    nsv6972336copy number variation1nstd229human GRCh38 chr15: 59,476,891-59,866,160 , GRCh37.p13 chr15: 59,769,090-60,158,359 GTF2A2, RPS3AP6, 7 more genes
    nsv6970942copy number variation1nstd229human GRCh38 chr15: 59,619,122-59,624,376 , GRCh37.p13 chr15: 59,911,321-59,916,575 GCNT3
    nsv6969701copy number variation1nstd229human GRCh38 chr15: 59,450,001-59,740,000 , GRCh37.p13 chr15: 59,742,200-60,032,199 GTF2A2, RPL21P114, 6 more genes
    nsv6967183copy number variation1nstd229human GRCh38 chr15: 59,586,641-59,615,143 , GRCh37.p13 chr15: 59,878,840-59,907,342 GCNT3
    nsv6964096copy number variation1nstd229human GRCh38 chr15: 59,517,162-59,616,839 , GRCh37.p13 chr15: 59,809,361-59,909,038 GCNT3, RPL21P117, 3 more genes
    nsv6958185copy number variation1nstd229human GRCh38 chr15: 59,566,873-59,637,210 , GRCh37.p13 chr15: 59,859,072-59,929,409 GTF2A2, GCNT3, 1 more genes
    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
    nsv6623130copy number variation1nstd224human GRCh37 chr15: 59,894,617-59,997,696 , GRCh38.p12 chr15: 59,602,418-59,705,497 BNIP2, GCNT3, 2 more genes
    nsv6586822inversion1nstd223human GRCh38 chr15: 59,615,251-60,468,567 , GRCh37.p13 chr15: 59,907,450-60,760,766 PIGHP1, MESTP2, 14 more genes
    nsv6515552copy number variation1nstd223human GRCh38 chr15: 59,586,641-59,615,140 , GRCh37.p13 chr15: 59,878,840-59,907,339 GCNT3
    nsv6501501copy number variation1nstd223human GRCh38 chr15: 59,619,122-59,624,373 , GRCh37.p13 chr15: 59,911,321-59,916,572 GCNT3
    nsv6249718mobile element insertion1nstd215human GRCh38 chr15: 59,611,025-59,611,025 , GRCh37.p13 chr15: 59,903,224-59,903,224 GCNT3
    nsv6202270copy number variation1nstd214human GRCh38 chr15: 59,610,181-59,610,232 , GRCh37.p13 chr15: 59,902,380-59,902,431 GCNT3
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