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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5977785insertion1nstd209human GRCh38 chr16: 52,577,732-52,577,732 , GRCh37.p13 chr16: 52,611,644-52,611,644 CASC16
    nsv5730879mobile element insertion1nstd211human GRCh38 chr16: 52,577,733-52,577,733 , GRCh37.p13 chr16: 52,611,645-52,611,645 CASC16
    nsv5562872inversion1nstd206human GRCh38 chr16: 52,564,001-52,575,383 , GRCh37.p13 chr16: 52,597,913-52,609,295 CASC16
    nsv5528085copy number variation1nstd206human GRCh38 chr16: 52,587,449-52,588,566 , GRCh37.p13 chr16: 52,621,361-52,622,478 CASC16, LOC105371265
    nsv5527739copy number variation1nstd206human GRCh38 chr16: 52,580,990-52,581,136 , GRCh37.p13 chr16: 52,614,902-52,615,048 CASC16, LOC105371265
    nsv5525286copy number variation1nstd206human GRCh38 chr16: 52,570,596-52,571,821 , GRCh37.p13 chr16: 52,604,508-52,605,733 CASC16
    nsv5358189translocation1nstd200human GRCh38 chr16: 52,570,596-52,570,596 , GRCh38 chr16: 52,571,821-52,571,821 , GRCh37.p13 chr16: 52,605,733-52,605,733 , GRCh37.p13 chr16: 52,604,508-52,604,508 CASC16
    nsv5182256mobile element insertion1nstd203human GRCh38 chr16: 52,577,732-52,577,732 , GRCh37.p13 chr16: 52,611,644-52,611,644 CASC16
    nsv5152742mobile element insertion1nstd203human GRCh38 chr16: 52,556,491-52,556,504 , GRCh37.p13 chr16: 52,590,403-52,590,416 CASC16
    nsv5033228inversion1nstd200human GRCh38 chr16: 52,564,001-52,575,379 , GRCh37.p13 chr16: 52,597,913-52,609,291 CASC16
    nsv5008249copy number variation1nstd200human GRCh38 chr16: 52,587,449-52,588,566 , GRCh37.p13 chr16: 52,621,361-52,622,478 CASC16, LOC105371265
    nsv5008248copy number variation1nstd200human GRCh38 chr16: 52,586,368-52,589,686 , GRCh37.p13 chr16: 52,620,280-52,623,598 LOC105371265, CASC16
    nsv5008247copy number variation1nstd200human GRCh38 chr16: 52,581,010-52,581,116 , GRCh37.p13 chr16: 52,614,922-52,615,028 LOC105371265, CASC16
    nsv4857118copy number variation1nstd200human GRCh37 chr16: 52,621,361-52,622,478 , GRCh38.p12 chr16: 52,587,449-52,588,566 CASC16, LOC105371265
    nsv4857117copy number variation1nstd200human GRCh37 chr16: 52,620,280-52,623,598 , GRCh38.p12 chr16: 52,586,368-52,589,686 CASC16, LOC105371265
    nsv4857116copy number variation1nstd200human GRCh37 chr16: 52,614,922-52,615,028 , GRCh38.p12 chr16: 52,581,010-52,581,116 CASC16, LOC105371265
    nsv4857115copy number variation1nstd200human GRCh37 chr16: 52,604,508-52,605,733 , GRCh38.p12 chr16: 52,570,596-52,571,821 CASC16
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4703498copy number variation1nstd195human GRCh38.p12 chr16: 52,341,189-52,955,989 , GRCh37 chr16: 52,375,101-52,989,901 TOX3, LOC146253, 7 more genes
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