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Items: 1 to 20 of 439

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6634772copy number variation1nstd227human GRCh37 chr7: 76,134,203-76,144,560 , GRCh38.p12 chr7: 76,504,886-76,515,243 , GRCh38.p12 chr7|NT_187561.1: 3,905-14,330 DTX2, UPK3B
    nsv6632444copy number variation1nstd224human GRCh37 chr7: 76,134,398-76,432,653 , GRCh38.p12 chr7: 76,505,081-76,803,336 , GRCh38.p12 chr7|NT_187561.1: 4,100-209,586 POMZP3, DTX2, 4 more genes
    nsv6632442copy number variation2nstd224human GRCh37 chr7: 76,131,646-76,144,561 , GRCh38.p12 chr7: 76,502,329-76,515,244 , GRCh38.p12 chr7|NT_187561.1: 1,348-14,331 UPK3B, DTX2
    nsv6632384copy number variation1nstd224human GRCh37 chr7: 76,134,398-76,452,331 , GRCh38.p12 chr7: 76,505,081-76,823,014 , GRCh38.p12 chr7|NT_187561.1: 4,100-209,586 POMZP3, DTX2, 4 more genes
    nsv6632181copy number variation1nstd224human GRCh37 chr7: 76,131,684-76,144,561 , GRCh38.p12 chr7: 76,502,367-76,515,244 , GRCh38.p12 chr7|NT_187561.1: 1,386-14,331 DTX2, UPK3B
    nsv6632006copy number variation1nstd224human GRCh37 chr7: 76,131,684-76,209,459 , GRCh38.p12 chr7: 76,502,367-76,580,142 , GRCh38.p12 chr7|NT_187561.1: 1,386-66,977 SPDYE1, UPK3B, 3 more genes
    nsv6303132copy number variation1nstd186human GRCh37 chr7: 76,208,715-76,213,048 , GRCh38.p12 chr7|NT_187561.1: 66,233-70,566 , GRCh38.p12 chr7: 76,579,398-76,583,731 LINC03009
    nsv6300991copy number variation1nstd186human GRCh37 chr7: 76,346,436-76,346,512 , GRCh38.p12 chr7: 76,717,119-76,717,195 , GRCh38.p12 chr7|NT_187561.1: 203,954-204,030
    nsv6292284mobile element insertion1nstd186human GRCh37 chr7: 76,334,070-76,334,121 , GRCh38.p12 chr7: 76,704,753-76,704,804 , GRCh38.p12 chr7|NT_187561.1: 191,588-191,639
    nsv5330276translocation1nstd200human GRCh37 chr7: 76,072,449-76,072,449 , GRCh37 chr7: 76,209,495-76,209,495 , GRCh38.p12 chr7: 76,580,178-76,580,178 , GRCh38.p12 chr7|NT_187561.1: 67,013-67,013 , GRCh38.p12 chr7: 76,443,132-76,443,132 LINC03009
    nsv4825082copy number variation1nstd200human GRCh37 chr7: 76,330,117-76,332,641 , GRCh38.p12 chr7|NT_187561.1: 187,635-190,159 , GRCh38.p12 chr7: 76,700,800-76,703,324
    nsv4811978copy number variation1nstd200human GRCh37 chr7: 76,251,029-76,253,595 , GRCh38.p12 chr7: 76,621,712-76,624,278 , GRCh38.p12 chr7|NT_187561.1: 108,547-111,113 POMZP3, LINC03009
    nsv4746065copy number variation1nstd199human GRCh37 chr7: 76,245,883-76,246,185 , GRCh38.p12 chr7: 76,616,566-76,616,868 , GRCh38.p12 chr7|NT_187561.1: 103,401-103,703 LINC03009, POMZP3
    nsv4742020copy number variation1nstd199human GRCh37 chr7: 76,209,674-76,209,731 , GRCh38.p12 chr7: 76,580,357-76,580,414 , GRCh38.p12 chr7|NT_187561.1: 67,192-67,249 LINC03009
    nsv4737809copy number variation1nstd199human GRCh37 chr7: 76,336,275-76,336,327 , GRCh38.p12 chr7: 76,706,958-76,707,010 , GRCh38.p12 chr7|NT_187561.1: 193,793-193,845
    nsv4728030copy number variation1nstd197human GRCh37 chr7: 76,240,783-76,241,130 , GRCh38.p12 chr7: 76,611,466-76,611,813 , GRCh38.p12 chr7|NT_187561.1: 98,301-98,648 POMZP3, LINC03009
    nsv4723056insertion1nstd186human GRCh37 chr7: 76,291,828-76,291,828 , GRCh38.p12 chr7: 76,662,511-76,662,511 , GRCh38.p12 chr7|NT_187561.1: 149,346-149,346
    nsv4690823mobile element insertion1nstd186human GRCh37 chr7: 76,291,838-76,291,838 , GRCh38.p12 chr7: 76,662,521-76,662,521 , GRCh38.p12 chr7|NT_187561.1: 149,356-149,356
    nsv4679108copy number variation1nstd189human GRCh37.p13 chr7: 76,123,485-76,521,617 , GRCh38.p12 chr7: 76,494,168-76,892,300 , GRCh38.p12 chr7|NT_187561.1: 1-209,586 , POMZP3, 7 more genes
    nsv4669307copy number variation1nstd186human GRCh37 chr7: 76,173,056-76,224,552 , GRCh38.p12 chr7: 76,543,739-76,595,235 , GRCh38.p12 chr7|NT_187561.1: 30,576-82,070 SPDYE1, LINC03009
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