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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5645001insertion1nstd207human GRCh38 chr17: 39,601,924-39,601,924 , GRCh37.p13 chr17: 37,758,177-37,758,177 NEUROD2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5156360mobile element insertion1nstd203human GRCh38 chr17: 39,604,760-39,604,795 , GRCh37.p13 chr17: 37,761,013-37,761,048 NEUROD2
    nsv5153680mobile element insertion1nstd203human GRCh38 chr17: 39,604,755-39,604,795 , GRCh37.p13 chr17: 37,761,008-37,761,048 NEUROD2
    nsv5016298copy number variation1nstd200human GRCh38 chr17: 39,607,547-39,607,692 , GRCh37.p13 chr17: 37,763,800-37,763,945 NEUROD2
    nsv4625569copy number variation1nstd183human GRCh37 chr17: 37,736,785-37,904,211 , GRCh38.p12 chr17: 39,580,532-39,747,958 ERBB2, PGAP3, 9 more genes
    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
    nsv4457589copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,190,609-37,868,002 , GRCh38.p12 chr17: 39,034,356-39,711,749 ERBB2, PGAP3, 23 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
    nsv3916479copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,521,822-37,768,345 , NCBI36 chr17: 34,775,348-35,021,871 , GRCh38 chr17: 39,365,569-39,612,092 CDK12, MED1, 5 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
    nsv3914774copy number variation1nstd102humanLikely benign GRCh38 chr17: 39,036,037-39,694,679 , NCBI36 chr17: 34,445,816-35,104,458 , GRCh37 chr17: 37,192,290-37,850,932 CDK12, PNMT, 23 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
    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
    nsv3903293copy number variation1nstd102humanUncertain significance GRCh37 chr17: 36,972,794-38,033,708 , GRCh38.p12 chr17: 38,816,541-39,877,455 LASP1NB, MED1, 46 more genes
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