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Items: 16

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    Number of Variants: 16

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3318841copy number variation6nstd157human GRCh37 chr10: 68,075,032-68,114,481 , GRCh38.p12 chr10: 66,315,274-66,354,723 CTNNA3
    nsv3318712copy number variation6nstd157human GRCh37 chr10: 6,655,306-6,663,988 , GRCh38.p12 chr10: 6,613,344-6,622,026 LINC02648
    nsv3318953copy number variation35nstd157human GRCh37 chr3: 53,032,639-53,038,786 , GRCh38.p12 chr3: 52,998,623-53,004,770 SFMBT1
    nsv3317135copy number variation14nstd157human GRCh37 chr11: 107,653,081-107,671,155 , GRCh38.p12 chr11: 107,782,355-107,800,429 SLC35F2
    nsv3318025copy number variation1nstd157human GRCh37 chr3: 155,479,723-155,497,571 , GRCh38.p12 chr3: 155,761,934-155,779,782 C3orf33
    nsv3317916copy number variation17nstd157human GRCh38.p12 chr15: 25,179,434-25,185,507 , GRCh37 chr15: 25,424,581-25,430,654 SNORD115-6, SNORD115-7, 3 more genes
    nsv3318201copy number variation1nstd157human GRCh38.p12 chr16: 24,992,864-25,061,852 , GRCh37 chr16: 25,004,185-25,073,173 ARHGAP17, LOC554206, 1 more genes
    nsv3318745copy number variation44nstd157human GRCh37 chr17: 34,438,753-34,483,342 , GRCh38.p12 chr17: 36,111,360-36,155,969 , GRCh38.p12 chr17|NT_187661.1: 65,457-110,066 , GRCh38.p12 chr17|NT_187614.1: 346,281-390,870 LOC100419980, LOC101927369, 2 more genes
    nsv3318446copy number variation4nstd157human GRCh37 chr5: 140,214,995-140,221,761 , GRCh38.p12 chr5: 140,835,410-140,842,176 PCDHA@, PCDHA8, 7 more genes
    nsv3318814copy number variation2nstd157human GRCh37 chr9: 10,660,982-10,688,528 , GRCh38.p12 chr9: 10,660,982-10,688,528 0
    nsv3318172copy number variation11nstd157human GRCh37 chr14: 86,285,493-86,312,888 , GRCh38.p12 chr14: 85,819,149-85,846,544 0
    nsv3317469copy number variation35nstd157human GRCh37 chr3: 65,189,366-65,214,533 , GRCh38.p12 chr3: 65,203,691-65,228,858 0
    nsv3317442copy number variation7nstd157human GRCh37 chr4: 161,048,496-161,072,119 , GRCh38.p12 chr4: 160,127,344-160,150,967 0
    nsv3317859copy number variation29nstd157human GRCh37 chr4: 64,136,609-64,154,477 , GRCh38.p12 chr4: 63,270,891-63,288,759 0
    nsv3318432copy number variation41nstd157human GRCh37 chr8: 5,595,511-5,605,706 , GRCh38.p12 chr8: 5,737,989-5,748,184 0
    nsv3317366copy number variation4nstd157human GRCh37 chr2: 106,347,912-106,353,107 , GRCh38.p12 chr2: 105,731,455-105,736,650 0
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