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Items: 1 to 20 of 436

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094860copy number variation1nstd102humanUncertain significance GRCh37 chr16: 69,728,151-69,731,549 , GRCh38.p12 chr16: 69,694,248-69,697,646 NFAT5
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7077835inversion1nstd229human GRCh38 chr16: 69,661,270-69,669,735 , GRCh37.p13 chr16: 69,695,173-69,703,638 NFAT5
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv7072044inversion1nstd229human GRCh38 chr16: 69,657,863-69,666,511 , GRCh37.p13 chr16: 69,691,766-69,700,414 NFAT5
    nsv7064268inversion1nstd229human GRCh38 chr16: 69,686,669-74,423,188 , GRCh37.p13 chr16: 69,720,572-74,457,086 LOC102723786, RNU7-90P, 99 more genes
    nsv7059282inversion1nstd229human GRCh38 chr16: 69,511,560-71,175,016 , GRCh37.p13 chr16: 69,545,463-71,208,919 COG4, DDX19B, 42 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6997663copy number variation1nstd229human GRCh38 chr16: 69,660,956-69,664,568 , GRCh37.p13 chr16: 69,694,859-69,698,471 NFAT5
    nsv6990311copy number variation1nstd229human GRCh38 chr16: 69,571,470-69,578,430 , GRCh37.p13 chr16: 69,605,373-69,612,333 NFAT5
    nsv6989767copy number variation1nstd229human GRCh38 chr16: 69,624,846-69,624,979 , GRCh37.p13 chr16: 69,658,749-69,658,882 NFAT5
    nsv6987911copy number variation1nstd229human GRCh38 chr16: 69,618,545-69,625,020 , GRCh37.p13 chr16: 69,652,448-69,658,923 NFAT5
    nsv6983071copy number variation1nstd229human GRCh38 chr16: 69,554,345-69,629,412 , GRCh37.p13 chr16: 69,588,248-69,663,315 MIR1538, NFAT5
    nsv6981758copy number variation1nstd229human GRCh38 chr16: 69,600,741-69,603,928 , GRCh37.p13 chr16: 69,634,644-69,637,831 NFAT5
    nsv6980681copy number variation1nstd229human GRCh38 chr16: 69,677,027-69,924,914 , GRCh37.p13 chr16: 69,710,930-69,958,817 NONOP1, SNORD13H, 4 more genes
    nsv6978831copy number variation1nstd229human GRCh38 chr16: 69,483,001-69,919,500 , GRCh37.p13 chr16: 69,516,904-69,953,403 NONOP1, SNORD13H, 6 more genes
    nsv6623740copy number variation1nstd224human GRCh37 chr16: 69,724,465-69,951,291 , GRCh38.p12 chr16: 69,690,562-69,917,388 NQO1, NFAT5, 4 more genes
    nsv6592699inversion1nstd223human GRCh38 chr16: 69,597,595-69,598,336 , GRCh37.p13 chr16: 69,631,498-69,632,239 NFAT5
    nsv6586732inversion1nstd223human GRCh38 chr16: 69,678,073-69,678,280 , GRCh37.p13 chr16: 69,711,976-69,712,183 NFAT5
    nsv6584197inversion1nstd223human GRCh38 chr16: 69,664,500-69,664,812 , GRCh37.p13 chr16: 69,698,403-69,698,715 NFAT5
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