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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055926inversion1nstd229human GRCh38 chr2: 223,723,053-227,096,551 , GRCh37.p13 chr2: 224,587,770-227,961,267 CUL3, MRPL44, 23 more genes
    nsv7047506inversion1nstd229human GRCh38 chr2: 222,618,340-223,958,759 , GRCh37.p13 chr2: 223,483,059-224,823,476 LOC105373903, LOC105373906, 22 more genes
    nsv7047209inversion1nstd229human GRCh38 chr2: 222,803,564-227,992,948 , GRCh37.p13 chr2: 223,668,283-228,857,664 MFF, LOC100289117, 55 more genes
    nsv7043640inversion1nstd229human GRCh38 chr2: 222,841,128-228,011,478 , GRCh37.p13 chr2: 223,705,846-228,876,194 MFF-DT, LOC105373905, 55 more genes
    nsv6694241copy number variation1nstd229human GRCh38 chr2: 223,887,550-223,935,617 , GRCh37.p13 chr2: 224,752,267-224,800,334 WDFY1, GTF3AP3
    nsv6693619copy number variation1nstd229human GRCh38 chr2: 223,862,117-224,002,420 , GRCh37.p13 chr2: 224,726,834-224,867,137 GTF3AP3, WDFY1, 2 more genes
    nsv6693307copy number variation1nstd229human GRCh38 chr2: 223,897,602-223,978,996 , GRCh37.p13 chr2: 224,762,319-224,843,713 MRPL44, GTF3AP3, 2 more genes
    nsv6690384copy number variation1nstd229human GRCh38 chr2: 223,917,273-223,917,357 , GRCh37.p13 chr2: 224,781,990-224,782,074 WDFY1
    nsv6687469copy number variation1nstd229human GRCh38 chr2: 223,943,489-223,978,642 , GRCh37.p13 chr2: 224,808,206-224,843,359 MRPL44, SERPINE2, 1 more genes
    nsv6685452copy number variation1nstd229human GRCh38 chr2: 223,942,027-223,942,138 , GRCh37.p13 chr2: 224,806,744-224,806,855 WDFY1
    nsv6682106copy number variation1nstd229human GRCh38 chr2: 223,796,152-223,889,591 , GRCh37.p13 chr2: 224,660,869-224,754,308 WDFY1, AP1S3
    nsv6682061copy number variation1nstd229human GRCh38 chr2: 223,942,160-223,996,919 , GRCh37.p13 chr2: 224,806,877-224,861,636 MRPL44, WDFY1, 1 more genes
    nsv6681576copy number variation1nstd229human GRCh38 chr2: 223,934,381-223,942,760 , GRCh37.p13 chr2: 224,799,098-224,807,477 WDFY1
    nsv6681357copy number variation1nstd229human GRCh38 chr2: 223,934,379-223,942,776 , GRCh37.p13 chr2: 224,799,096-224,807,493 WDFY1
    nsv6680889copy number variation1nstd229human GRCh38 chr2: 223,924,437-223,929,081 , GRCh37.p13 chr2: 224,789,154-224,793,798 WDFY1
    nsv6541339inversion1nstd223human GRCh38 chr2: 223,881,738-223,882,354 , GRCh37.p13 chr2: 224,746,455-224,747,071 WDFY1
    nsv6538647inversion1nstd223human GRCh38 chr2: 223,896,175-223,897,372 , GRCh37.p13 chr2: 224,760,892-224,762,089 WDFY1
    nsv6352445copy number variation1nstd223human GRCh38 chr2: 223,875,501-223,876,600 , GRCh37.p13 chr2: 224,740,218-224,741,317 WDFY1
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315345copy number variation1nstd102humanPathogenic GRCh37 chr2: 222,902,251-226,084,516 , GRCh38.p12 chr2: 222,037,532-225,219,799 LOC105373911, LOC105373908, 43 more genes
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