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Items: 1 to 20 of 321

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554903sequence alteration1nstd206human GRCh38 chr17: 662,533-1,370,380 , GRCh37.p13 chr17: 565,773-1,273,674 , YWHAE, 19 more genes
    nsv5374766translocation1nstd200human GRCh38 chr17: 998,869-998,869 , GRCh38 chr17: 1,017,097-1,017,097 , GRCh37.p13 chr17: 920,337-920,337 , GRCh37.p13 chr17: 902,109-902,109 ABR, TIMM22
    nsv5343517translocation1nstd200human GRCh37 chr17: 920,337-920,337 , GRCh37 chr17: 902,109-902,109 , GRCh38.p12 chr17: 1,017,097-1,017,097 , GRCh38.p12 chr17|NT_187664.1: 56,344-56,344 , GRCh38.p12 chr17|NT_187664.1: 38,116-38,116 , GRCh38.p12 chr17|NT_187613.1: 56,344-56,344 , GRCh38.p12 chr17: 998,869-998,869 , GRCh38.p12 chr17|NT_187613.1: 38,116-38,116 ABR, TIMM22
    nsv5314730copy number variation1nstd204human GRCh38.p13 chr17: 914,606-1,283,637 , GRCh37.p13 chr17: 817,846-1,186,931 , 11 more genes
    nsv5013646copy number variation1nstd200human GRCh38 chr17: 990,035-1,018,868 , GRCh37.p13 chr17: 893,275-922,108 , LOC105371481, 2 more genes
    nsv5013638copy number variation1nstd200human GRCh38 chr17: 883,020-1,069,726 , GRCh37.p13 chr17: 786,260-972,966 , ABR, 5 more genes
    nsv4864431copy number variation1nstd200human GRCh37 chr17: 893,275-922,108 , GRCh38.p12 chr17|NT_187613.1: 29,282-58,115 , GRCh38.p12 chr17: 990,035-1,018,868 , GRCh38.p12 chr17|NT_187664.1: 29,282-58,115 , ABR, 2 more genes
    nsv4864427copy number variation1nstd200human GRCh37 chr17: 817,855-1,186,923 , GRCh38.p12 chr17: 914,615-1,283,629 , GRCh38.p12 chr17|NT_187613.1: 1-238,838 , TIMM22, 11 more genes
    nsv4769394copy number variation1nstd102humanUncertain significance GRCh37 chr17: 722,145-1,875,784 , GRCh38.p12 chr17: 818,905-1,972,490 SCARF1, WDR81, 31 more genes
    nsv4768381copy number variation1nstd102humanPathogenic GRCh37 chr17: 84,287-2,468,384 , GRCh38.p12 chr17: 234,496-2,565,090 GLOD4, RTN4RL1, 67 more genes
    nsv4768380copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 1-1,026,797 , GRCh38.p12 chr17: 150,208-1,123,462 ABR, DOC2B, 19 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729775copy number variation1nstd102humanUncertain significance GRCh37 chr17: 111,222-964,297 , GRCh38.p12 chr17: 261,431-1,061,057 TLCD3A, GLOD4, 17 more genes
    nsv4729765copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-1,450,120 , GRCh38.p12 chr17: 150,732-1,546,826 LOC105371425, PITPNA-AS1, 31 more genes
    nsv4678884copy number variation1nstd189human GRCh37.p13 chr17: 216,719-963,064 , GRCh38.p12 chr17: 366,928-1,059,824 , ABR, 15 more genes
    nsv4675624copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-2,221,159 , GRCh38.p12 chr17: 150,732-2,317,865 HNRNPA1P16, RTN4RL1, 60 more genes
    nsv4675586copy number variation1nstd102humanUncertain significance GRCh37 chr17: 279,703-1,154,012 , GRCh38.p12 chr17: 429,912-1,250,718 RPS4XP17, LOC105371480, 15 more genes
    nsv4675245copy number variation1nstd102humanUncertain significance GRCh37 chr17: 699,175-981,413 , GRCh38.p12 chr17: 795,935-1,078,173 ABR, TIMM22, 4 more genes
    nsv4675207copy number variation1nstd102humanUncertain significance GRCh37 chr17: 525-969,410 , GRCh38.p12 chr17: 150,732-1,066,170 LOC105371481, TLCD3A, 19 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
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