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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914518copy number variation1nstd209human GRCh38 chr7: 75,772,667-75,773,177 , GRCh37.p13 chr7|NW_003871064.1: 3,301,903-3,302,413 , GRCh37.p13 chr7: 75,401,985-75,402,495 CCL26
    nsv5911264copy number variation1nstd209human GRCh38 chr7: 75,787,404-75,791,029 , GRCh37.p13 chr7|NW_003871064.1: 3,316,640-3,320,265 , GRCh37.p13 chr7: 75,416,722-75,420,347 CCL26
    nsv5863474copy number variation1nstd209human GRCh38 chr7: 75,786,922-75,791,053 , GRCh37.p13 chr7: 75,416,240-75,420,371 , GRCh37.p13 chr7|NW_003871064.1: 3,316,158-3,320,289 CCL26
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493871copy number variation1nstd206human GRCh38 chr7: 75,775,045-75,778,865 , GRCh37.p13 chr7: 75,404,363-75,408,183 , GRCh37.p13 chr7|NW_003871064.1: 3,304,281-3,308,101 CCL26
    nsv5491367copy number variation1nstd206human GRCh38 chr7: 75,770,392-75,770,727 , GRCh37.p13 chr7: 75,399,710-75,400,045 , GRCh37.p13 chr7|NW_003871064.1: 3,299,628-3,299,963 CCL26
    nsv5491289copy number variation1nstd206human GRCh38 chr7: 75,787,364-75,791,014 , GRCh37.p13 chr7|NW_003871064.1: 3,316,600-3,320,250 , GRCh37.p13 chr7: 75,416,682-75,420,332 CCL26
    nsv5487966copy number variation1nstd206human GRCh38 chr7: 75,789,219-75,790,481 , GRCh37.p13 chr7|NW_003871064.1: 3,318,455-3,319,717 , GRCh37.p13 chr7: 75,418,537-75,419,799 CCL26
    nsv5482490copy number variation1nstd206human GRCh38 chr7: 75,787,415-75,797,294 , GRCh37.p13 chr7: 75,416,733-75,426,612 , GRCh37.p13 chr7|NW_003871064.1: 3,316,651-3,326,530 CCL26
    nsv5481893copy number variation1nstd206human GRCh38 chr7: 75,699,833-75,789,513 , GRCh37.p13 chr7|NW_003871064.1: 3,229,069-3,318,749 , GRCh37.p13 chr7: 75,329,151-75,418,831 CCL26, HIP1
    nsv5363850translocation1nstd200human GRCh38 chr7: 75,791,014-75,791,014 , GRCh38 chr7: 75,787,364-75,787,364 , GRCh37.p13 chr7: 75,420,332-75,420,332 , GRCh37.p13 chr7|NW_003871064.1: 3,320,250-3,320,250 , GRCh37.p13 chr7: 75,416,682-75,416,682 , GRCh37.p13 chr7|NW_003871064.1: 3,316,600-3,316,600 CCL26
    nsv5237259copy number variation1nstd204human GRCh38.p13 chr7: 75,762,001-75,770,300 , GRCh37.p13 chr7|NW_003871064.1: 3,291,237-3,299,536 , GRCh37.p13 chr7: 75,391,319-75,399,618 CCL26
    nsv5228367copy number variation1nstd204human GRCh38.p13 chr7: 75,787,297-75,790,953 , GRCh37.p13 chr7: 75,416,615-75,420,271 , GRCh37.p13 chr7|NW_003871064.1: 3,316,533-3,320,189 CCL26
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4950104copy number variation1nstd200human GRCh38 chr7: 75,778,936-75,788,166 , GRCh37.p13 chr7: 75,408,254-75,417,484 , GRCh37.p13 chr7|NW_003871064.1: 3,308,172-3,317,402 CCL26
    nsv4950103copy number variation1nstd200human GRCh38 chr7: 75,779,053-75,781,600 , GRCh37.p13 chr7|NW_003871064.1: 3,308,289-3,310,836 , GRCh37.p13 chr7: 75,408,371-75,410,918 CCL26
    nsv4950102copy number variation1nstd200human GRCh38 chr7: 75,767,130-75,802,061 , GRCh37.p13 chr7: 75,396,448-75,431,379 , GRCh37.p13 chr7|NW_003871064.1: 3,296,366-3,331,297 CCL26
    nsv4950101copy number variation1nstd200human GRCh38 chr7: 75,764,594-75,768,464 , GRCh37.p13 chr7: 75,393,912-75,397,782 , GRCh37.p13 chr7|NW_003871064.1: 3,293,830-3,297,700 CCL26
    nsv4950100copy number variation1nstd200human GRCh38 chr7: 75,764,147-75,768,325 , GRCh37.p13 chr7|NW_003871064.1: 3,293,383-3,297,561 , GRCh37.p13 chr7: 75,393,465-75,397,643 CCL26
    nsv4811940copy number variation1nstd200human GRCh37 chr7: 75,408,371-75,410,918 , GRCh38.p12 chr7: 75,779,053-75,781,600 CCL26
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