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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5871421copy number variation1nstd209human GRCh38 chr1: 177,145,820-177,148,436 , GRCh37.p13 chr1: 177,114,956-177,117,572 ASTN1
    nsv5828559copy number variation1nstd209human GRCh38 chr1: 177,145,793-177,148,297 , GRCh37.p13 chr1: 177,114,929-177,117,433 ASTN1
    nsv5719761mobile element insertion1nstd211human GRCh38 chr1: 176,989,516-176,989,516 , GRCh37.p13 chr1: 176,958,652-176,958,652 ASTN1
    nsv5683901mobile element insertion2nstd211human GRCh38 chr1: 177,079,271-177,079,271 , GRCh37.p13 chr1: 177,048,407-177,048,407 ASTN1
    nsv5678959mobile element insertion1nstd211human GRCh38 chr1: 177,071,422-177,071,422 , GRCh37.p13 chr1: 177,040,558-177,040,558 ASTN1
    nsv5618263insertion1nstd207human GRCh38 chr1: 177,149,662-177,149,662 , GRCh37.p13 chr1: 177,118,798-177,118,798 ASTN1
    nsv5609050insertion1nstd207human GRCh38 chr1: 177,149,371-177,149,371 , GRCh37.p13 chr1: 177,118,507-177,118,507 ASTN1
    nsv5583082copy number variation1nstd207human GRCh38 chr1: 177,149,634-177,149,773 , GRCh37.p13 chr1: 177,118,770-177,118,909 ASTN1
    nsv5569692copy number variation1nstd207human GRCh38 chr1: 177,149,662-177,149,717 , GRCh37.p13 chr1: 177,118,798-177,118,853 ASTN1
    nsv5558405mobile element insertion1nstd206human GRCh38 chr1: 176,989,516-176,989,567 , GRCh37.p13 chr1: 176,958,652-176,958,703 ASTN1
    nsv5430421copy number variation1nstd206human GRCh38 chr1: 176,725,110-176,926,077 , GRCh37.p13 chr1: 176,694,246-176,895,213 ASTN1, PAPPA2
    nsv5424978copy number variation1nstd206human GRCh38 chr1: 177,156,394-177,156,712 , GRCh37.p13 chr1: 177,125,530-177,125,848 ASTN1
    nsv5422033copy number variation1nstd206human GRCh38 chr1: 176,905,640-176,905,700 , GRCh37.p13 chr1: 176,874,776-176,874,836 ASTN1
    nsv5421359copy number variation1nstd206human GRCh38 chr1: 177,145,822-177,148,437 , GRCh37.p13 chr1: 177,114,958-177,117,573 ASTN1
    nsv5420500copy number variation1nstd206human GRCh38 chr1: 177,105,121-177,105,496 , GRCh37.p13 chr1: 177,074,257-177,074,632 ASTN1
    nsv5418446copy number variation1nstd206human GRCh38 chr1: 177,104,866-177,105,087 , GRCh37.p13 chr1: 177,074,002-177,074,223 ASTN1
    nsv5408796mobile element insertion1nstd206human GRCh38 chr1: 177,079,271-177,079,322 , GRCh37.p13 chr1: 177,048,407-177,048,458 ASTN1
    nsv5399398mobile element insertion1nstd206human GRCh38 chr1: 177,071,422-177,071,473 , GRCh37.p13 chr1: 177,040,558-177,040,609 ASTN1
    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
    nsv5364312translocation1nstd200human GRCh38 chr6: 68,622,435-68,622,435 , GRCh38 chr1: 176,956,543-176,956,543 , GRCh37.p13 chr1: 176,925,679-176,925,679 , GRCh37.p13 chr6: 69,332,327-69,332,327 ASTN1
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