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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6125745copy number variation1nstd186human GRCh37 chr17: 26,843,857-26,844,213 , GRCh38.p12 chr17: 28,516,839-28,517,195 FOXN1
    nsv5652547insertion1nstd207human GRCh38 chr17: 28,517,647-28,517,647 , GRCh37.p13 chr17: 26,844,665-26,844,665 FOXN1
    nsv5600339copy number variation1nstd207human GRCh38 chr17: 28,517,579-28,517,646 , GRCh37.p13 chr17: 26,844,597-26,844,664 FOXN1
    nsv5600229copy number variation1nstd207human GRCh38 chr17: 28,517,647-28,517,867 , GRCh37.p13 chr17: 26,844,665-26,844,885 FOXN1
    nsv5599453copy number variation1nstd207human GRCh38 chr17: 28,516,649-28,516,987 , GRCh37.p13 chr17: 26,843,667-26,844,005 FOXN1
    nsv5594975copy number variation1nstd207human GRCh38 chr17: 28,516,878-28,516,978 , GRCh37.p13 chr17: 26,843,896-26,843,996 FOXN1
    nsv5533200copy number variation1nstd206human GRCh38 chr17: 28,522,526-28,522,730 , GRCh37.p13 chr17: 26,849,544-26,849,748 FOXN1
    nsv5530632copy number variation1nstd206human GRCh38 chr17: 28,519,923-28,523,621 , GRCh37.p13 chr17: 26,846,941-26,850,639 FOXN1
    nsv5528104copy number variation1nstd206human GRCh38 chr17: 28,516,839-28,517,195 , GRCh37.p13 chr17: 26,843,857-26,844,213 FOXN1
    nsv5391660copy number variation1nstd186human GRCh37 chr17: 26,843,799-26,844,102 , GRCh38.p12 chr17: 28,516,781-28,517,084 FOXN1
    nsv5390813copy number variation1nstd186human GRCh37 chr17: 26,843,624-26,844,011 , GRCh38.p12 chr17: 28,516,606-28,516,993 FOXN1
    nsv5358775translocation1nstd200human GRCh38 chr17: 28,518,687-28,518,687 , GRCh38 chr17: 28,518,768-28,518,768 , GRCh37.p13 chr17: 26,845,786-26,845,786 , GRCh37.p13 chr17: 26,845,705-26,845,705 FOXN1
    nsv5324347copy number variation1nstd204human GRCh38.p13 chr17: 28,516,549-28,517,374 , GRCh37.p13 chr17: 26,843,567-26,844,392 FOXN1
    nsv5322111copy number variation1nstd204human GRCh38.p13 chr17: 28,517,573-28,518,116 , GRCh37.p13 chr17: 26,844,591-26,845,134 FOXN1
    nsv5292666copy number variation1nstd204human GRCh38.p13 chr17: 28,515,928-28,517,367 , GRCh37.p13 chr17: 26,842,946-26,844,385 FOXN1
    nsv5143799mobile element insertion1nstd203human GRCh38 chr17: 28,507,110-28,507,110 , GRCh37.p13 chr17: 26,834,128-26,834,128 , GRCh37.p13 chr17|NW_003871090.1: 188,971-188,971 FOXN1
    nsv5023902copy number variation1nstd200human GRCh38 chr17: 28,371,101-28,759,758 , GRCh37.p13 chr17: 26,840,020-27,086,776 RSKR, TRAF4, 26 more genes
    nsv5010254copy number variation1nstd200human GRCh38 chr17: 28,516,603-28,516,996 , GRCh37.p13 chr17: 26,843,621-26,844,014 FOXN1
    nsv4858463copy number variation1nstd200human GRCh37 chr17: 26,846,941-26,850,639 , GRCh38.p12 chr17: 28,519,923-28,523,621 FOXN1
    nsv4858462copy number variation1nstd200human GRCh37 chr17: 26,843,650-26,844,231 , GRCh38.p12 chr17: 28,516,632-28,517,213 FOXN1
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