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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5013830copy number variation1nstd200human GRCh38 chr17: 53,639,912-53,968,349 , GRCh37.p13 chr17: 51,717,273-52,045,710 LOC107984982, KIF2B, 2 more genes
    nsv4676365copy number variation1nstd102humanUncertain significance GRCh37 chr17: 51,852,844-51,920,768 , GRCh38.p12 chr17: 53,775,483-53,843,407 KIF2B
    nsv4632353copy number variation1nstd183human GRCh37 chr17: 51,792,073-52,040,215 , GRCh38.p12 chr17: 53,714,712-53,962,854 KIF2B, RPS2P48, 2 more genes
    nsv4457639copy number variation1nstd102humanUncertain significance GRCh37 chr17: 51,564,311-52,793,787 , GRCh38.p12 chr17: 53,486,950-54,716,426 RPS2P48, LOC107985001, 4 more genes
    nsv4387117copy number variation1nstd173human GRCh37 chr17: 51,715,300-52,043,990 , GRCh38.p12 chr17: 53,637,939-53,966,629 LOC100128713, RPS2P48, 2 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
    nsv3922974copy number variation1nstd102humanUncertain significance GRCh37 chr17: 51,771,501-52,059,263 , GRCh38 chr17: 53,694,140-53,981,902 , NCBI36 chr17: 49,126,500-49,414,262 LOC100128713, LOC107985001, 3 more genes
    nsv3920880copy number variation1nstd102humanPathogenic GRCh38 chr17: 49,974,533-56,807,609 , NCBI36 chr17: 45,406,896-52,239,969 , GRCh37 chr17: 48,051,897-54,884,970 LOC107984983, LOC102724732, 85 more genes
    nsv3916185copy number variation1nstd102humanUncertain significance GRCh37 chr17: 51,653,200-52,729,855 , GRCh38 chr17: 53,575,839-54,652,494 , NCBI36 chr17: 49,008,199-50,084,854 KIF2B, LOC107984982, 4 more genes
    nsv3915195copy number variation1nstd102humanUncertain significance NCBI36 chr17: 49,008,254-50,084,867 , GRCh38 chr17: 53,575,894-54,652,507 , GRCh37 chr17: 51,653,255-52,729,868 KIF2B, LOC107984982, 4 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
    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
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