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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556253sequence alteration1nstd206human GRCh37.p13 chr17: 43,035,798-43,218,336 , GRCh38 chr17: 44,958,430-45,140,969 NMT1, C1QL1, 6 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv4531936copy number variation1nstd166human GRCh37.p13 chr17: 43,040,656-43,041,162 , GRCh38.p12 chr17: 44,963,288-44,963,794 C1QL1
    nsv4337950sequence alteration1nstd166human GRCh37.p13 chr17: 43,030,318-43,044,629 , GRCh38.p12 chr17: 44,952,950-44,967,261 C1QL1
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3920797copy number variation1nstd102humanPathogenic GRCh37 chr17: 43,005,866-43,377,096 , NCBI36 chr17: 40,361,392-40,732,879 , GRCh38 chr17: 44,928,498-45,299,730 HEXIM2, KIF18B, 18 more genes
    nsv3918486copy number variation1nstd102humanUncertain significance GRCh38 chr17: 44,906,235-45,220,406 , NCBI36 chr17: 40,339,129-40,653,556 , GRCh37 chr17: 42,983,603-43,297,773 GFAP, MIR6783, 16 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
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 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
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
    nsv3899474copy number variation1nstd102humanUncertain significance GRCh37 chr17: 42,649,083-43,659,985 , GRCh38.p12 chr17: 44,571,715-45,582,619 PLEKHM1, HIGD1B, 45 more genes
    esv4010335copy number variation1estd233human GRCh37 chr17: 41,468,000-43,513,000 , GRCh38.p12 chr17: 43,390,632-45,435,634 , ARL4D, 102 more genes
    nsv2786099copy number variation1nstd132human NCBI36 chr17: 40,332,718-40,717,274 , GRCh37.p13 chr17: 42,977,192-43,361,491 , GRCh38.p12 chr17: 44,899,824-45,284,124 GFAP, PLCD3, 23 more genes
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