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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5875778copy number variation1nstd209human GRCh38 chr1: 33,152,438-33,154,668 , GRCh37.p13 chr1: 33,618,039-33,620,269 TRIM62, AZIN2
    nsv5829998copy number variation1nstd209human GRCh38 chr1: 33,152,800-33,154,699 , GRCh37.p13 chr1: 33,618,401-33,620,300 AZIN2, TRIM62
    nsv5727965mobile element insertion1nstd211human GRCh38 chr1: 33,128,704-33,128,704 , GRCh37.p13 chr1: 33,594,305-33,594,305 AZIN2
    nsv5556023mobile element insertion1nstd206human GRCh38 chr1: 33,128,704-33,128,755 , GRCh37.p13 chr1: 33,594,305-33,594,356 AZIN2
    nsv5430377copy number variation1nstd206human GRCh38 chr1: 33,122,152-33,122,223 , GRCh37.p13 chr1: 33,587,753-33,587,824 AZIN2
    nsv5424410copy number variation1nstd206human GRCh38 chr1: 33,080,387-33,080,460 , GRCh37.p13 chr1: 33,545,988-33,546,061 AZIN2, LOC105378635
    nsv5414438copy number variation1nstd206human GRCh38 chr1: 33,148,847-33,150,987 , GRCh37.p13 chr1: 33,614,448-33,616,588 AZIN2, TRIM62
    nsv5361133translocation1nstd200human GRCh38 chr1: 33,148,510-33,148,510 , GRCh38 chr1: 33,148,437-33,148,437 , GRCh37.p13 chr1: 33,614,111-33,614,111 , GRCh37.p13 chr1: 33,614,038-33,614,038 TRIM62, AZIN2
    nsv5361132translocation1nstd200human GRCh38 chr1: 33,122,223-33,122,223 , GRCh38 chr1: 33,122,152-33,122,152 , GRCh37.p13 chr1: 33,587,753-33,587,753 , GRCh37.p13 chr1: 33,587,824-33,587,824 AZIN2
    nsv5361131translocation1nstd200human GRCh38 chr1: 33,080,387-33,080,387 , GRCh38 chr1: 33,080,461-33,080,461 , GRCh37.p13 chr1: 33,545,988-33,545,988 , GRCh37.p13 chr1: 33,546,062-33,546,062 AZIN2, LOC105378635
    nsv5341853translocation1nstd200human GRCh37 chr1: 33,587,753-33,587,753 , GRCh37 chr1: 33,587,824-33,587,824 , GRCh38.p12 chr1: 33,122,152-33,122,152 , GRCh38.p12 chr1: 33,122,223-33,122,223 AZIN2
    nsv4903342copy number variation1nstd200human GRCh38 chr1: 33,034,541-33,209,384 , GRCh37.p13 chr1: 33,500,142-33,674,985 , LOC105378635, 3 more genes
    nsv4895862copy number variation1nstd200human GRCh38 chr1: 33,098,182-33,103,823 , GRCh37.p13 chr1: 33,563,783-33,569,424 AZIN2
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4728269copy number variation1nstd102humanUncertain significance GRCh37 chr1: 33,490,421-33,599,915 , GRCh38.p12 chr1: 33,024,820-33,134,314 LOC105378635, AK2, 1 more genes
    nsv4674454copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 30,819,875-34,380,419 , GRCh38.p12 chr1: 30,347,028-33,914,818 AK2, ADGRB2, 97 more genes
    nsv4563805mobile element insertion1nstd166human GRCh37.p13 chr1: 33,613,732-33,613,732 , GRCh38.p12 chr1: 33,148,131-33,148,131 AZIN2, TRIM62
    nsv4460829mobile element insertion1nstd166human GRCh37.p13 chr1: 33,608,185-33,608,185 , GRCh38.p12 chr1: 33,142,584-33,142,584 AZIN2
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