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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5880957copy number variation1nstd209human GRCh38 chr1: 205,374,044-205,379,774 , GRCh37.p13 chr1: 205,343,172-205,348,902 LEMD1, LEMD1-AS1, 1 more genes
    nsv5877862copy number variation1nstd209human GRCh38 chr1: 205,411,147-205,411,205 , GRCh37.p13 chr1: 205,380,275-205,380,333 LEMD1
    nsv5829096copy number variation1nstd209human GRCh38 chr1: 205,374,042-205,379,957 , GRCh37.p13 chr1: 205,343,170-205,349,085 LOC105371698, LEMD1-AS1, 1 more genes
    nsv5692693mobile element insertion2nstd211human GRCh38 chr1: 205,414,041-205,414,041 , GRCh37.p13 chr1: 205,383,169-205,383,169 LEMD1
    nsv5623578insertion1nstd207human GRCh38 chr1: 205,411,133-205,411,133 , GRCh37.p13 chr1: 205,380,261-205,380,261 LEMD1
    nsv5443342copy number variation1nstd206human GRCh38 chr1: 205,416,696-205,423,398 , GRCh37.p13 chr1: 205,385,824-205,392,526 LEMD1
    nsv5437339copy number variation1nstd206human GRCh38 chr1: 205,411,126-205,411,216 , GRCh37.p13 chr1: 205,380,254-205,380,344 LEMD1
    nsv5404850mobile element insertion1nstd206human GRCh38 chr1: 205,414,041-205,414,092 , GRCh37.p13 chr1: 205,383,169-205,383,220 LEMD1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5210146copy number variation1nstd204human GRCh38.p13 chr1: 205,437,401-205,442,500 , GRCh37.p13 chr1: 205,406,529-205,411,628 LEMD1, BLACAT1
    nsv5062267mobile element insertion1nstd203human GRCh38 chr1: 205,414,025-205,414,041 , GRCh37.p13 chr1: 205,383,153-205,383,169 LEMD1
    nsv4904276copy number variation1nstd200human GRCh38 chr1: 205,368,397-205,441,281 , GRCh37.p13 chr1: 205,337,525-205,410,409 LEMD1-AS1, LEMD1, 2 more genes
    nsv4898347copy number variation1nstd200human GRCh38 chr1: 205,423,669-205,424,796 , GRCh37.p13 chr1: 205,392,797-205,393,924 LEMD1
    nsv4898346copy number variation1nstd200human GRCh38 chr1: 205,423,576-205,425,267 , GRCh37.p13 chr1: 205,392,704-205,394,395 LEMD1
    nsv4789346copy number variation1nstd200human GRCh37 chr1: 205,392,704-205,394,391 , GRCh38.p12 chr1: 205,423,576-205,425,263 LEMD1
    nsv4789345copy number variation1nstd200human GRCh37 chr1: 205,380,067-205,380,850 , GRCh38.p12 chr1: 205,410,939-205,411,722 LEMD1
    nsv4774106copy number variation1nstd200human GRCh37 chr1: 205,392,797-205,393,924 , GRCh38.p12 chr1: 205,423,669-205,424,796 LEMD1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4753597insertion1nstd199human GRCh37 chr1: 205,380,208-205,380,208 , GRCh38.p12 chr1: 205,411,080-205,411,080 LEMD1
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
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