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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
    nsv5940699copy number variation1nstd209human GRCh38 chr13: 77,710,476-77,879,918 , GRCh37.p13 chr13: 78,284,611-78,454,053 , SLAIN1, 1 more genes
    nsv5927933copy number variation1nstd209human GRCh38 chr13: 77,881,824-77,885,515 , GRCh37.p13 chr13: 78,455,959-78,459,650 EDNRB-AS1
    nsv5862376copy number variation1nstd209human GRCh38 chr13: 77,904,473-77,908,085 , GRCh37.p13 chr13: 78,478,608-78,482,220 EDNRB, EDNRB-AS1
    nsv5854012copy number variation1nstd209human GRCh38 chr13: 77,882,359-77,885,558 , GRCh37.p13 chr13: 78,456,494-78,459,693 EDNRB-AS1
    nsv5699735mobile element insertion2nstd211human GRCh38 chr13: 77,837,396-77,837,396 , GRCh37.p13 chr13: 78,411,531-78,411,531 EDNRB-AS1
    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
    nsv5596250copy number variation1nstd207human GRCh38 chr13: 77,881,824-77,885,512 , GRCh37.p13 chr13: 78,455,959-78,459,647 EDNRB-AS1
    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
    nsv5513647copy number variation1nstd206human GRCh38 chr13: 77,881,824-77,885,516 , GRCh37.p13 chr13: 78,455,959-78,459,651 EDNRB-AS1
    nsv5503128copy number variation1nstd206human GRCh38 chr13: 77,849,356-77,849,412 , GRCh37.p13 chr13: 78,423,491-78,423,547 EDNRB-AS1
    nsv5502223copy number variation1nstd206human GRCh38 chr13: 77,817,306-77,817,365 , GRCh37.p13 chr13: 78,391,441-78,391,500 , EDNRB-AS1
    nsv5501041copy number variation1nstd206human GRCh38 chr13: 77,875,391-77,875,448 , GRCh37.p13 chr13: 78,449,526-78,449,583 EDNRB-AS1
    nsv5498061copy number variation1nstd206human GRCh38 chr13: 77,904,551-77,908,373 , GRCh37.p13 chr13: 78,478,686-78,482,508 EDNRB-AS1, EDNRB
    nsv5433204mobile element insertion1nstd206human GRCh38 chr13: 77,837,396-77,837,447 , GRCh37.p13 chr13: 78,411,531-78,411,582 EDNRB-AS1
    nsv5307846copy number variation1nstd204human GRCh38.p13 chr13: 77,883,827-77,886,128 , GRCh37.p13 chr13: 78,457,962-78,460,263 EDNRB-AS1
    nsv5302626copy number variation1nstd204human GRCh38.p13 chr13: 77,881,819-77,885,522 , GRCh37.p13 chr13: 78,455,954-78,459,657 EDNRB-AS1
    nsv5279113copy number variation1nstd204human GRCh38.p13 chr13: 77,881,801-77,885,500 , GRCh37.p13 chr13: 78,455,936-78,459,635 EDNRB-AS1
    nsv5276948copy number variation1nstd204human GRCh38.p13 chr13: 77,883,801-77,886,100 , GRCh37.p13 chr13: 78,457,936-78,460,235 EDNRB-AS1
    nsv5276597copy number variation1nstd204human GRCh38.p13 chr13: 77,885,201-77,886,100 , GRCh37.p13 chr13: 78,459,336-78,460,235 EDNRB-AS1
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