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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5946351copy number variation1nstd209human GRCh38 chr17: 35,938,646-35,938,695 , GRCh37.p13 chr17: 34,265,650-34,265,699 LYZL6
    nsv5703481mobile element insertion2nstd211human GRCh38 chr17: 35,934,565-35,934,565 , GRCh37.p13 chr17: 34,261,569-34,261,569 LYZL6
    nsv5698193mobile element insertion1nstd211human GRCh38 chr17: 35,943,377-35,943,377 , GRCh37.p13 chr17: 34,270,381-34,270,381 LYZL6
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5432923mobile element insertion1nstd206human GRCh38 chr17: 35,943,377-35,943,428 , GRCh37.p13 chr17: 34,270,381-34,270,432 LYZL6
    nsv5425415mobile element insertion1nstd206human GRCh38 chr17: 35,934,565-35,934,616 , GRCh37.p13 chr17: 34,261,569-34,261,620 LYZL6
    nsv5156214mobile element insertion1nstd203human GRCh38 chr17: 35,934,553-35,934,561 , GRCh37.p13 chr17: 34,261,557-34,261,565 LYZL6
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675787copy number variation1nstd102humanUncertain significance GRCh37 chr17: 34,158,619-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 CCL4, CCL3-AS1, 15 more genes
    nsv4634127copy number variation1nstd183human GRCh37 chr17: 34,151,274-34,485,091 , GRCh38.p12 chr17: 35,919,249-36,157,718 , GRCh38.p12 chr17|NT_187614.1: 153,781-392,619 , RDM1, 16 more genes
    nsv4631441copy number variation1nstd183human GRCh37 chr17: 34,149,960-34,475,514 , GRCh38.p12 chr17: 35,919,249-36,148,133 , GRCh38.p12 chr17|NT_187614.1: 153,781-383,042 , CCL14, 16 more genes
    nsv4502413mobile element insertion1nstd166human GRCh37.p13 chr17: 34,261,557-34,261,557 , GRCh38.p12 chr17|NT_187614.1: 169,085-169,085 , GRCh38.p12 chr17: 35,934,553-35,934,553 LYZL6
    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
    nsv4457542copy number variation1nstd102humanUncertain significance GRCh37 chr17: 34,151,183-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 CCL14, LOC101927369, 15 more genes
    nsv4380150copy number variation1nstd173human GRCh37 chr17: 34,151,081-34,477,480 , GRCh38.p12 chr17: 35,919,249-36,150,098 , GRCh38.p12 chr17|NT_187614.1: 153,781-385,008 , CCL4, 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
    nsv3967213insertion1nstd168human GRCh38 chr17: 35,936,461-35,952,582 , GRCh37.p13 chr17: 34,263,465-34,279,586 LYZL6
    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
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