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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5941141copy number variation1nstd209human GRCh38 chr13: 77,904,551-77,908,369 , GRCh37.p13 chr13: 78,478,686-78,482,504 EDNRB, EDNRB-AS1
    nsv5937509copy number variation1nstd209human GRCh38 chr13: 77,966,143-77,966,213 , GRCh37.p13 chr13: 78,540,278-78,540,348 EDNRB
    nsv5933603copy number variation1nstd209human GRCh38 chr13: 77,938,419-77,938,478 , GRCh37.p13 chr13: 78,512,554-78,512,613 EDNRB
    nsv5932186copy number variation1nstd209human GRCh38 chr13: 77,934,881-83,910,012 , GRCh37.p13 chr13: 78,509,016-84,484,147 NDFIP2, LINC01068, 54 more genes
    nsv5927950copy number variation1nstd209human GRCh38 chr13: 77,961,176-77,961,281 , GRCh37.p13 chr13: 78,535,311-78,535,416 EDNRB
    nsv5862376copy number variation1nstd209human GRCh38 chr13: 77,904,473-77,908,085 , GRCh37.p13 chr13: 78,478,608-78,482,220 EDNRB, EDNRB-AS1
    nsv5723624mobile element insertion1nstd211human GRCh38 chr13: 77,965,730-77,965,730 , GRCh37.p13 chr13: 78,539,865-78,539,865 EDNRB
    nsv5672806copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr13: 77,566,087-78,492,734 , GRCh38.p12 chr13: 76,991,952-77,918,599 LOC107984564, MYCBP2-AS1, 13 more genes
    nsv5662985insertion1nstd207human GRCh38 chr13: 77,942,673-77,942,673 , GRCh37.p13 chr13: 78,516,808-78,516,808 EDNRB
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5555861mobile element insertion1nstd206human GRCh38 chr13: 77,965,730-77,965,781 , GRCh37.p13 chr13: 78,539,865-78,539,916 EDNRB
    nsv5512608copy number variation1nstd206human GRCh38 chr13: 77,961,380-77,962,057 , GRCh37.p13 chr13: 78,535,515-78,536,192 EDNRB
    nsv5502062copy number variation1nstd206human GRCh38 chr13: 77,929,559-77,935,458 , GRCh37.p13 chr13: 78,503,694-78,509,593 EDNRB
    nsv5499309copy number variation1nstd206human GRCh38 chr13: 77,933,395-77,939,216 , GRCh37.p13 chr13: 78,507,530-78,513,351 EDNRB
    nsv5498061copy number variation1nstd206human GRCh38 chr13: 77,904,551-77,908,373 , GRCh37.p13 chr13: 78,478,686-78,482,508 EDNRB-AS1, EDNRB
    nsv5348737translocation1nstd200human GRCh38 chr13: 77,935,458-77,935,458 , GRCh38 chr13: 77,929,559-77,929,559 , GRCh37.p13 chr13: 78,509,593-78,509,593 , GRCh37.p13 chr13: 78,503,694-78,503,694 EDNRB
    nsv5314954copy number variation1nstd204human GRCh38.p13 chr13: 77,929,552-77,935,467 , GRCh37.p13 chr13: 78,503,687-78,509,602 EDNRB
    nsv5277819copy number variation1nstd204human GRCh38.p13 chr13: 77,929,477-77,935,170 , GRCh37.p13 chr13: 78,503,612-78,509,305 EDNRB
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv5008880copy number variation1nstd200human GRCh38 chr13: 77,933,511-77,939,345 , GRCh37.p13 chr13: 78,507,646-78,513,480 EDNRB
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