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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099264copy number variation1nstd231human GRCh38.p12 chr1: 222,151,895-226,849,338 , GRCh37 chr1: 222,325,237-227,037,039 PARP1, CAPN2, 99 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv6675709copy number variation1nstd229human GRCh38 chr1: 224,161,301-224,385,400 , GRCh37.p13 chr1: 224,349,003-224,573,102 LOC101927164, FBXO28, 8 more genes
    nsv6673745copy number variation1nstd229human GRCh38 chr1: 224,162,401-224,287,000 , GRCh37.p13 chr1: 224,350,103-224,474,702 LOC724084, LOC101927143, 5 more genes
    nsv6671058copy number variation1nstd229human GRCh38 chr1: 224,145,831-224,146,060 , GRCh37.p13 chr1: 224,333,533-224,333,762 FBXO28
    nsv6670529copy number variation1nstd229human GRCh38 chr1: 224,125,301-224,128,053 , GRCh37.p13 chr1: 224,313,003-224,315,755 FBXO28
    nsv6669235copy number variation1nstd229human GRCh38 chr1: 224,136,574-224,139,553 , GRCh37.p13 chr1: 224,324,276-224,327,255 FBXO28
    nsv6667248copy number variation1nstd229human GRCh38 chr1: 224,150,237-224,151,956 , GRCh37.p13 chr1: 224,337,939-224,339,658 FBXO28
    nsv6666669copy number variation1nstd229human GRCh38 chr1: 224,102,696-224,112,218 , GRCh37.p13 chr1: 224,290,398-224,299,920 FBXO28, LOC105373056, 1 more genes
    nsv6663880copy number variation1nstd229human GRCh38 chr1: 224,142,276-224,145,135 , GRCh37.p13 chr1: 224,329,978-224,332,837 FBXO28
    nsv6663831copy number variation1nstd229human GRCh38 chr1: 224,102,643-224,112,203 , GRCh37.p13 chr1: 224,290,345-224,299,905 FBXO28, LOC105373056, 1 more genes
    nsv6663450copy number variation1nstd229human GRCh38 chr1: 224,135,401-224,139,700 , GRCh37.p13 chr1: 224,323,103-224,327,402 FBXO28
    nsv6659606copy number variation1nstd229human GRCh38 chr1: 224,147,988-224,148,484 , GRCh37.p13 chr1: 224,335,690-224,336,186 FBXO28
    nsv6659276copy number variation1nstd229human GRCh38 chr1: 224,115,580-224,116,057 , GRCh37.p13 chr1: 224,303,282-224,303,759 FBXO28
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636736copy number variation1nstd102humanUncertain significance GRCh37 chr1: 221,325,488-225,804,228 , GRCh38.p12 chr1: 221,152,146-225,616,526 BROX, LINC02765, 77 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6554411inversion1nstd223human GRCh38 chr1: 224,139,055-224,139,765 , GRCh37.p13 chr1: 224,326,757-224,327,467 FBXO28
    nsv6545139inversion1nstd223human GRCh38 chr1: 224,132,782-224,133,556 , GRCh37.p13 chr1: 224,320,484-224,321,258 FBXO28
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