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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146204insertion1nstd232human GRCh37.p13 chr13: 80,113,910-80,113,910 , GRCh38.p12 chr13: 79,539,775-79,539,775 NDFIP2
    nsv7073631inversion1nstd229human GRCh38 chr13: 79,487,394-79,487,433 , GRCh37.p13 chr13: 80,061,529-80,061,568 NDFIP2
    nsv7065657inversion1nstd229human GRCh38 chr13: 76,225,150-84,243,039 , GRCh37.p13 chr13: 76,799,286-84,817,174 HSPD1P8, ELOCP23, 85 more genes
    nsv7064226inversion1nstd229human GRCh38 chr13: 79,480,333-84,336,702 , GRCh37.p13 chr13: 80,054,468-84,910,837 LINC01038, LOC105370287, 32 more genes
    nsv7061790inversion1nstd229human GRCh38 chr13: 76,348,646-84,254,120 , GRCh37.p13 chr13: 76,922,782-84,828,255 LINC01068, LOC105370264, 83 more genes
    nsv6956831copy number variation1nstd229human GRCh38 chr13: 79,553,201-79,576,000 , GRCh37.p13 chr13: 80,127,336-80,150,135 NDFIP2, LINC01068
    nsv6952210copy number variation1nstd229human GRCh38 chr13: 79,485,891-79,486,049 , GRCh37.p13 chr13: 80,060,026-80,060,184 NDFIP2
    nsv6951765copy number variation1nstd229human GRCh38 chr13: 79,512,077-79,616,461 , GRCh37.p13 chr13: 80,086,212-80,190,596 NDFIP2, LINC01068
    nsv6948816copy number variation1nstd229human GRCh38 chr13: 79,478,459-79,618,354 , GRCh37.p13 chr13: 80,052,594-80,192,489 NDFIP2-AS1, NDFIP2, 1 more genes
    nsv6947172copy number variation1nstd229human GRCh38 chr13: 79,556,532-79,557,861 , GRCh37.p13 chr13: 80,130,667-80,131,996 NDFIP2
    nsv6945823copy number variation1nstd229human GRCh38 chr13: 79,531,003-79,531,203 , GRCh37.p13 chr13: 80,105,138-80,105,338 NDFIP2
    nsv6940502copy number variation1nstd229human GRCh38 chr13: 79,507,257-79,507,573 , GRCh37.p13 chr13: 80,081,392-80,081,708 NDFIP2
    nsv6939079copy number variation1nstd229human GRCh38 chr13: 79,480,301-79,488,400 , GRCh37.p13 chr13: 80,054,436-80,062,535 NDFIP2, NDFIP2-AS1
    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
    nsv6637820copy number variation1nstd102humanUncertain significance GRCh37 chr13: 79,099,535-80,675,355 , GRCh38.p12 chr13: 78,525,400-80,101,220 LINC00382, CCT5-2P, 21 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
    nsv6495467copy number variation1nstd223human GRCh38 chr13: 79,541,001-79,542,100 , GRCh37.p13 chr13: 80,115,136-80,116,235 NDFIP2
    nsv6494648copy number variation1nstd223human GRCh38 chr13: 79,492,303-79,495,359 , GRCh37.p13 chr13: 80,066,438-80,069,494 NDFIP2
    nsv6490696copy number variation1nstd223human GRCh38 chr13: 79,544,601-79,545,600 , GRCh37.p13 chr13: 80,118,736-80,119,735 NDFIP2
    nsv6486041copy number variation1nstd223human GRCh38 chr13: 79,552,766-79,557,636 , GRCh37.p13 chr13: 80,126,901-80,131,771 NDFIP2
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