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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945814copy number variation1nstd209human GRCh38 chr13: 49,917,451-49,917,534 , GRCh37.p13 chr13: 50,491,587-50,491,670 SPRYD7
    nsv5935626copy number variation1nstd209human GRCh38 chr13: 49,931,496-49,931,559 , GRCh37.p13 chr13: 50,505,632-50,505,695 SPRYD7
    nsv5858956copy number variation1nstd209human GRCh38 chr13: 49,911,896-49,913,770 , GRCh37.p13 chr13: 50,486,032-50,487,906 SPRYD7
    nsv5856554copy number variation1nstd209human GRCh38 chr13: 49,916,662-49,917,961 , GRCh37.p13 chr13: 50,490,798-50,492,097 SPRYD7
    nsv5695978mobile element insertion1nstd211human GRCh38 chr13: 49,915,359-49,915,359 , GRCh37.p13 chr13: 50,489,495-50,489,495 SPRYD7
    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
    nsv5511628copy number variation1nstd206human GRCh38 chr13: 49,922,027-49,922,169 , GRCh37.p13 chr13: 50,496,163-50,496,305 SPRYD7
    nsv5509830copy number variation1nstd206human GRCh38 chr13: 49,928,677-49,928,730 , GRCh37.p13 chr13: 50,502,813-50,502,866 SPRYD7
    nsv5500213copy number variation1nstd206human GRCh38 chr13: 49,911,439-49,913,745 , GRCh37.p13 chr13: 50,485,575-50,487,881 SPRYD7
    nsv5500169copy number variation1nstd206human GRCh38 chr13: 49,922,296-49,922,350 , GRCh37.p13 chr13: 50,496,432-50,496,486 SPRYD7
    nsv5496630copy number variation1nstd206human GRCh38 chr13: 49,917,451-49,917,535 , GRCh37.p13 chr13: 50,491,587-50,491,671 SPRYD7
    nsv5307050copy number variation1nstd204human GRCh38.p13 chr13: 49,201,982-51,085,310 , GRCh37.p13 chr13: 49,776,118-51,659,446 , MLNR, 40 more genes
    nsv5263460copy number variation1nstd204human GRCh38.p13 chr13: 49,908,870-49,917,161 , GRCh37.p13 chr13: 50,483,006-50,491,297 SPRYD7, RNY4P9
    nsv5261616copy number variation1nstd204human GRCh38.p13 chr13: 49,936,001-49,940,900 , GRCh37.p13 chr13: 50,510,137-50,515,036 SPRYD7
    nsv5183155mobile element insertion1nstd203human GRCh38 chr13: 49,930,265-49,930,274 , GRCh37.p13 chr13: 50,504,401-50,504,410 SPRYD7
    nsv5152587mobile element insertion1nstd203human GRCh38 chr13: 49,924,438-49,924,452 , GRCh37.p13 chr13: 50,498,574-50,498,588 SPRYD7
    nsv4997442copy number variation1nstd200human GRCh38 chr13: 49,927,262-49,930,311 , GRCh37.p13 chr13: 50,501,398-50,504,447 SPRYD7
    nsv4997441copy number variation1nstd200human GRCh38 chr13: 49,922,027-49,922,169 , GRCh37.p13 chr13: 50,496,163-50,496,305 SPRYD7
    nsv4997440copy number variation1nstd200human GRCh38 chr13: 49,911,408-49,913,746 , GRCh37.p13 chr13: 50,485,544-50,487,882 SPRYD7
    nsv4997437copy number variation1nstd200human GRCh38 chr13: 49,852,848-49,918,883 , GRCh37.p13 chr13: 50,426,984-50,493,019 SPRYD7, RNY4P30, 2 more genes
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