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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944562copy number variation1nstd209human GRCh38 chr17: 29,540,718-29,873,240 , GRCh37.p13 chr17: 27,867,736-28,200,258 RPL21P123, GIT1, 10 more genes
    nsv5023927copy number variation1nstd200human GRCh38 chr17: 29,564,920-29,579,708 , GRCh37.p13 chr17: 27,891,938-27,906,726 GIT1, TP53I13, 1 more genes
    nsv4864597copy number variation1nstd200human GRCh37 chr17: 27,891,938-27,906,726 , GRCh38.p12 chr17: 29,564,920-29,579,708 TP53I13, ABHD15, 1 more genes
    nsv4864596copy number variation1nstd200human GRCh37 chr17: 27,867,683-28,200,332 , GRCh38.p12 chr17: 29,540,665-29,873,314 ANKRD13B, TAOK1, 10 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729763copy number variation1nstd102humanUncertain significance GRCh37 chr17: 27,573,641-28,206,747 , GRCh38.p12 chr17: 29,246,623-29,879,729 GIT1, RPL21P123, 17 more genes
    nsv4675321copy number variation1nstd102humanPathogenic GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689 ABHD15, LOC100420408, 112 more genes
    nsv4629120copy number variation1nstd183human GRCh37 chr17: 27,893,704-27,896,005 , GRCh38.p12 chr17: 29,566,686-29,568,987 ABHD15, TP53I13
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 more genes
    nsv4370646copy number variation1nstd173human GRCh37 chr17: 27,870,962-28,495,223 , GRCh38.p12 chr17: 29,543,944-30,168,205 RNU6-920P, ABHD15, 16 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4247658copy number variation1nstd166human GRCh37.p13 chr17: 27,895,138-27,895,674 , GRCh38.p12 chr17: 29,568,120-29,568,656 TP53I13
    nsv3972367copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 25,403,446-31,685,464 , GRCh38.p12 chr17: 27,076,420-33,358,446 ASIC2, AK4P1, 190 more genes
    nsv3919950copy number variation1nstd102humanPathogenic NCBI36 chr17: 24,298,969-27,841,151 , GRCh37 chr17: 27,274,843-30,817,038 , GRCh38 chr17: 28,947,825-32,490,020 MIR365B, EFCAB5, 105 more genes
    nsv3916884copy number variation1nstd102humanUncertain significance NCBI36 chr17: 24,137,711-25,589,217 , GRCh37.p13 chr17: 27,113,585-28,565,091 , GRCh38.p12 chr17: 28,786,567-30,238,073 MIR451B, SEZ6, 43 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
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