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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143367copy number variation1nstd232human GRCh37.p13 chr13: 91,148,116-91,148,214 , GRCh38.p12 chr13: 90,495,862-90,495,960 LINC01049
    nsv7142103insertion1nstd232human GRCh37.p13 chr13: 91,149,408-91,149,408 , GRCh38.p12 chr13: 90,497,154-90,497,154 LINC01049
    nsv7065549inversion1nstd229human GRCh38 chr13: 90,505,522-90,505,765 , GRCh37.p13 chr13: 91,157,776-91,158,019 LINC01049
    nsv7063899inversion1nstd229human GRCh38 chr13: 87,663,888-92,195,406 , GRCh37.p13 chr13: 88,316,143-92,847,659 RNU6-75P, LOC105370311, 50 more genes
    nsv6957744copy number variation1nstd229human GRCh38 chr13: 90,530,756-90,530,856 , GRCh37.p13 chr13: 91,183,010-91,183,110 LINC01049
    nsv6953943copy number variation1nstd229human GRCh38 chr13: 90,525,077-90,527,531 , GRCh37.p13 chr13: 91,177,331-91,179,785 LINC01049
    nsv6953675copy number variation1nstd229human GRCh38 chr13: 90,385,725-91,323,552 , GRCh37.p13 chr13: 91,037,979-91,975,806 LOC105370312, PPIAP23, 10 more genes
    nsv6952270copy number variation1nstd229human GRCh38 chr13: 90,423,361-90,506,011 , GRCh37.p13 chr13: 91,075,615-91,158,265 LINC01049
    nsv6951710copy number variation1nstd229human GRCh38 chr13: 90,507,784-90,508,033 , GRCh37.p13 chr13: 91,160,038-91,160,287 LINC01049
    nsv6949060copy number variation1nstd229human GRCh38 chr13: 90,529,215-90,530,952 , GRCh37.p13 chr13: 91,181,469-91,183,206 LINC01049
    nsv6942260copy number variation1nstd229human GRCh38 chr13: 90,514,571-90,534,599 , GRCh37.p13 chr13: 91,166,825-91,186,853 LINC01049
    nsv6940141copy number variation1nstd229human GRCh38 chr13: 90,532,870-90,543,572 , GRCh37.p13 chr13: 91,185,124-91,195,826 LINC01049
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637507copy number variation1nstd102humanUncertain significance GRCh37 chr13: 86,667,980-91,833,689 , GRCh38.p12 chr13: 86,093,845-91,181,435 LINC00559, LOC105370304, 47 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6492298copy number variation1nstd223human GRCh38 chr13: 90,530,201-90,532,700 , GRCh37.p13 chr13: 91,182,455-91,184,954 LINC01049
    nsv6484803copy number variation1nstd223human GRCh38 chr13: 90,515,401-90,516,100 , GRCh37.p13 chr13: 91,167,655-91,168,354 LINC01049
    nsv6484527copy number variation1nstd223human GRCh38 chr13: 90,524,801-90,528,300 , GRCh37.p13 chr13: 91,177,055-91,180,554 LINC01049
    nsv6479488copy number variation1nstd223human GRCh38 chr13: 90,521,883-90,522,364 , GRCh37.p13 chr13: 91,174,137-91,174,618 LINC01049
    nsv6476622copy number variation1nstd223human GRCh38 chr13: 90,508,966-90,509,758 , GRCh37.p13 chr13: 91,161,220-91,162,012 LINC01049
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