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Items: 1 to 20 of 467

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145241copy number variation1nstd232human GRCh37.p13 chr14: 99,986,774-99,986,834 , GRCh38.p12 chr14: 99,520,437-99,520,497 CCDC85C
    nsv7144453copy number variation1nstd232human GRCh37.p13 chr14: 99,986,789-99,986,901 , GRCh38.p12 chr14: 99,520,452-99,520,564 CCDC85C
    nsv6974295copy number variation1nstd229human GRCh38 chr14: 99,514,590-99,531,584 , GRCh37.p13 chr14: 99,980,927-99,997,921 CCDC85C
    nsv6973993copy number variation1nstd229human GRCh38 chr14: 99,538,217-99,541,098 , GRCh37.p13 chr14: 100,004,554-100,007,435 CCDC85C, LOC105370661
    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
    nsv6971254copy number variation1nstd229human GRCh38 chr14: 99,538,528-99,541,281 , GRCh37.p13 chr14: 100,004,865-100,007,618 LOC105370661, CCDC85C
    nsv6971126copy number variation1nstd229human GRCh38 chr14: 99,528,815-99,577,281 , GRCh37.p13 chr14: 99,995,152-100,043,618 LOC105370661, CCDC85C
    nsv6970465copy number variation1nstd229human GRCh38 chr14: 99,559,236-99,591,056 , GRCh37.p13 chr14: 100,025,573-100,057,393 CCDC85C
    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
    nsv6967177copy number variation1nstd229human GRCh38 chr14: 99,502,453-99,502,520 , GRCh37.p13 chr14: 99,968,790-99,968,857 CCNK, CCDC85C
    nsv6965785copy number variation1nstd229human GRCh38 chr14: 99,590,133-99,592,480 , GRCh37.p13 chr14: 100,056,470-100,058,817 CCDC85C
    nsv6964331copy number variation1nstd229human GRCh38 chr14: 99,537,901-99,550,000 , GRCh37.p13 chr14: 100,004,238-100,016,337 LOC105370661, CCDC85C
    nsv6962761copy number variation1nstd229human GRCh38 chr14: 99,537,196-99,567,918 , GRCh37.p13 chr14: 100,003,533-100,034,255 CCDC85C, LOC105370661
    nsv6961824copy number variation1nstd229human GRCh38 chr14: 99,589,471-99,600,117 , GRCh37.p13 chr14: 100,055,808-100,066,454 CCDC85C
    nsv6959236copy number variation1nstd229human GRCh38 chr14: 99,582,254-99,590,391 , GRCh37.p13 chr14: 100,048,591-100,056,728 CCDC85C
    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
    nsv6507944copy number variation1nstd223human GRCh38 chr14: 99,571,493-99,584,928 , GRCh37.p13 chr14: 100,037,830-100,051,265 CCDC85C
    nsv6504185copy number variation1nstd223human GRCh38 chr14: 99,528,815-99,577,278 , GRCh37.p13 chr14: 99,995,152-100,043,615 LOC105370661, CCDC85C
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