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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130624insertion1nstd186human GRCh37 chr16: 66,839,386-66,839,386 , GRCh38.p12 chr16: 66,805,483-66,805,483 NAE1
    nsv5698836mobile element insertion1nstd211human GRCh38 chr16: 66,817,915-66,817,915 , GRCh37.p13 chr16: 66,851,818-66,851,818 NAE1
    nsv5550355insertion1nstd206human GRCh38 chr16: 66,805,483-66,805,483 , GRCh37.p13 chr16: 66,839,386-66,839,386 NAE1
    nsv5427201mobile element insertion1nstd206human GRCh38 chr16: 66,817,915-66,817,917 , GRCh37.p13 chr16: 66,851,818-66,851,820 NAE1
    nsv5308695copy number variation1nstd204human GRCh38.p13 chr16: 66,807,645-66,808,369 , GRCh37.p13 chr16: 66,841,548-66,842,272 NAE1
    nsv5157486mobile element insertion1nstd203human GRCh38 chr16: 66,805,484-66,805,496 , GRCh37.p13 chr16: 66,839,387-66,839,399 NAE1
    nsv5154147mobile element insertion1nstd203human GRCh38 chr16: 66,805,483-66,805,500 , GRCh37.p13 chr16: 66,839,386-66,839,403 NAE1
    nsv5152322mobile element insertion1nstd203human GRCh38 chr16: 66,805,487-66,805,500 , GRCh37.p13 chr16: 66,839,390-66,839,403 NAE1
    nsv5152116mobile element insertion1nstd203human GRCh38 chr16: 66,830,302-66,830,314 , GRCh37.p13 chr16: 66,864,205-66,864,217 NAE1
    nsv5146796mobile element insertion1nstd203human GRCh38 chr16: 66,805,496-66,805,496 , GRCh37.p13 chr16: 66,839,399-66,839,399 NAE1
    nsv5144066mobile element insertion1nstd203human GRCh38 chr16: 66,805,489-66,805,500 , GRCh37.p13 chr16: 66,839,392-66,839,403 NAE1
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005774copy number variation1nstd200human GRCh38 chr16: 66,826,846-66,827,180 , GRCh37.p13 chr16: 66,860,749-66,861,083 NAE1
    nsv5005773copy number variation1nstd200human GRCh38 chr16: 66,784,994-66,812,680 , GRCh37.p13 chr16: 66,818,897-66,846,583 NAE1, TERB1
    nsv4993075copy number variation1nstd200human GRCh38 chr16: 66,828,989-66,829,169 , GRCh37.p13 chr16: 66,862,892-66,863,072 NAE1
    nsv4878809inversion1nstd200human GRCh37 chr16: 60,132,255-77,533,939 , GRCh38.p12 chr16: 60,098,351-77,500,042 , ST3GAL2, 313 more genes
    nsv4864200copy number variation1nstd200human GRCh37 chr16: 66,860,749-66,861,083 , GRCh38.p12 chr16: 66,826,846-66,827,180 NAE1
    nsv4857456copy number variation1nstd200human GRCh37 chr16: 66,862,892-66,863,072 , GRCh38.p12 chr16: 66,828,989-66,829,169 NAE1
    nsv4752587insertion1nstd199human GRCh37 chr16: 66,839,388-66,839,388 , GRCh38.p12 chr16: 66,805,485-66,805,485 NAE1
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
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