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Items: 1 to 20 of 173

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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
    nsv5727761mobile element insertion1nstd211human GRCh38 chr1: 33,180,388-33,180,388 , GRCh37.p13 chr1: 33,645,989-33,645,989 TRIM62
    nsv5559260mobile element insertion1nstd206human GRCh38 chr1: 33,180,388-33,180,439 , GRCh37.p13 chr1: 33,645,989-33,646,040 TRIM62
    nsv5433319copy number variation1nstd206human GRCh38 chr1: 33,183,923-33,187,272 , GRCh37.p13 chr1: 33,649,524-33,652,873 TRIM62
    nsv5421556copy number variation1nstd206human GRCh38 chr1: 33,180,860-33,180,986 , GRCh37.p13 chr1: 33,646,461-33,646,587 TRIM62
    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
    nsv4903342copy number variation1nstd200human GRCh38 chr1: 33,034,541-33,209,384 , GRCh37.p13 chr1: 33,500,142-33,674,985 , LOC105378635, 3 more genes
    nsv4895864copy number variation1nstd200human GRCh38 chr1: 33,183,923-33,187,272 , GRCh37.p13 chr1: 33,649,524-33,652,873 TRIM62
    nsv4895863copy number variation1nstd200human GRCh38 chr1: 33,170,453-33,174,034 , GRCh37.p13 chr1: 33,636,054-33,639,635 TRIM62
    nsv4772999copy number variation1nstd200human GRCh37 chr1: 33,649,524-33,652,873 , GRCh38.p12 chr1: 33,183,923-33,187,272 TRIM62
    nsv4772998copy number variation1nstd200human GRCh37 chr1: 33,636,054-33,639,635 , GRCh38.p12 chr1: 33,170,453-33,174,034 TRIM62
    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
    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
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4375461copy number variation1nstd173human GRCh37 chr1: 32,893,553-33,643,361 , GRCh38.p12 chr1: 32,427,952-33,177,760 , RPL18AP4, 22 more genes
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