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Items: 14

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    Number of Variants: 14

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6620234copy number variation1nstd224human GRCh37 chr10: 117,226,750-117,278,786 , GRCh38.p12 chr10: 115,467,240-115,519,276 ATRNL1
    nsv6631770copy number variation1nstd224human GRCh37 chr7: 133,136,872-133,171,749 , GRCh38.p12 chr7: 133,452,118-133,486,995 EXOC4
    nsv6626041copy number variation1nstd224human GRCh37 chr1: 62,692,092-62,718,827 , GRCh38.p12 chr1: 62,226,420-62,253,155 KANK4
    nsv6622934copy number variation1nstd224human GRCh37 chr14: 99,182,535-99,202,206 , GRCh38.p12 chr14: 98,716,198-98,735,869 LINC02914
    nsv6626588copy number variation3nstd224human GRCh37 chr20: 58,440,438-58,461,828 , GRCh38.p12 chr20: 59,865,383-59,886,773 SYCP2
    nsv6629971copy number variation4nstd224human GRCh37 chr4: 69,679,570-69,708,718 , GRCh38.p12 chr4: 68,813,852-68,843,000 LOC100422189, UGT2B10
    nsv6625326copy number variation12nstd224human GRCh37 chr19: 6,961,182-7,014,437 , GRCh38.p12 chr19: 6,961,171-7,014,426 ADGRE4P, LOC112268245, 1 more genes
    nsv6631041copy number variation21nstd224human GRCh37 chr6: 31,360,255-31,453,618 , GRCh38.p12 chr6: 31,392,478-31,485,841 HCP5, HLA-X, 5 more genes
    nsv6625759copy number variation3nstd224human GRCh37 chr1: 12,921,311-13,187,294 , GRCh38.p12 chr1: 12,861,456-13,119,821 PRAMEF25, PRAMEF27, 12 more genes
    nsv6632180copy number variation8nstd224human GRCh37 chr7: 76,131,646-76,561,369 , GRCh38.p12 chr7: 76,502,329-76,932,052 POMZP3, DTX2, 4 more genes
    nsv6622369copy number variation248nstd224human GRCh37 chr14: 20,213,937-20,420,151 , GRCh38.p12 chr14: 19,745,778-19,951,992 OR4N1P, OR4K1, 10 more genes
    nsv6623615copy number variation320nstd224human GRCh37 chr16: 34,516,075-34,686,820 , GRCh38.p12 chr16: 35,281,704-35,452,449 AGGF1P4, FRG2IP, 14 more genes
    nsv6628383copy number variation49nstd224human GRCh37 chr2: 57,416,841-57,445,471 , GRCh38.p12 chr2: 57,189,706-57,218,336 0
    nsv6632147copy number variation132nstd224human GRCh37 chr7: 44,935-67,365 , GRCh38.p12 chr7: 44,935-67,365 , GRCh38.p12 chr7|NT_187558.1: 1,034-23,464 , GRCh38.p12 chr7|NT_187653.1: 37,256-59,686 0
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