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Items: 1 to 20 of 508

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145260copy number variation1nstd232human GRCh37.p13 chr14: 100,123,161-100,123,231 , GRCh38.p12 chr14: 99,656,824-99,656,894 HHIPL1
    nsv7073074inversion1nstd229human GRCh38 chr14: 99,646,022-99,727,066 , GRCh37.p13 chr14: 100,112,359-100,193,403 CYP46A1, HHIPL1
    nsv7061481inversion1nstd229human GRCh38 chr14: 99,636,307-99,645,440 , GRCh37.p13 chr14: 100,102,644-100,111,777 HHIPL1
    nsv6975872copy number variation1nstd229human GRCh38 chr14: 99,672,325-99,680,063 , GRCh37.p13 chr14: 100,138,662-100,146,400 HHIPL1
    nsv6973056copy number variation1nstd229human GRCh38 chr14: 99,480,601-99,659,800 , GRCh37.p13 chr14: 99,946,938-100,126,137 CCNK, SETD3, 3 more genes
    nsv6972475copy number variation1nstd229human GRCh38 chr14: 99,175,901-99,949,300 , GRCh37.p13 chr14: 99,642,238-100,415,637 SETD3, LOC105370661, 10 more genes
    nsv6972243copy number variation1nstd229human GRCh38 chr14: 98,444,126-100,047,287 , GRCh37.p13 chr14: 98,910,463-100,513,624 CYP46A1, RPS2P3, 19 more genes
    nsv6972192copy number variation1nstd229human GRCh38 chr14: 99,656,839-99,656,895 , GRCh37.p13 chr14: 100,123,176-100,123,232 HHIPL1
    nsv6972127copy number variation1nstd229human GRCh38 chr14: 99,637,556-99,643,851 , GRCh37.p13 chr14: 100,103,893-100,110,188 HHIPL1
    nsv6971448copy number variation1nstd229human GRCh38 chr14: 99,677,934-99,678,345 , GRCh37.p13 chr14: 100,144,271-100,144,682 HHIPL1
    nsv6969080copy number variation1nstd229human GRCh38 chr14: 99,647,118-99,652,273 , GRCh37.p13 chr14: 100,113,455-100,118,610 HHIPL1
    nsv6968993copy number variation1nstd229human GRCh38 chr14: 99,650,224-99,680,817 , GRCh37.p13 chr14: 100,116,561-100,147,154 HHIPL1
    nsv6968255copy number variation1nstd229human GRCh38 chr14: 99,175,601-99,684,700 , GRCh37.p13 chr14: 99,641,938-100,151,037 BCL11B, CCDC85C, 7 more genes
    nsv6967961copy number variation1nstd229human GRCh38 chr14: 99,607,094-99,613,345 , GRCh37.p13 chr14: 100,073,431-100,079,682 HHIPL1
    nsv6963064copy number variation1nstd229human GRCh38 chr14: 99,606,742-99,615,596 , GRCh37.p13 chr14: 100,073,079-100,081,933 HHIPL1
    nsv6962101copy number variation1nstd229human GRCh38 chr14: 99,636,867-99,637,481 , GRCh37.p13 chr14: 100,103,204-100,103,818 HHIPL1
    nsv6960784copy number variation1nstd229human GRCh38 chr14: 99,675,201-99,684,800 , GRCh37.p13 chr14: 100,141,538-100,151,137 HHIPL1, CYP46A1
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6590551inversion1nstd223human GRCh38 chr14: 99,646,022-99,727,066 , GRCh37.p13 chr14: 100,112,359-100,193,403 CYP46A1, HHIPL1
    nsv6513792copy number variation1nstd223human GRCh38 chr14: 99,607,047-99,613,344 , GRCh37.p13 chr14: 100,073,384-100,079,681 HHIPL1
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