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Items: 1 to 20 of 89

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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
    nsv5149816mobile element insertion1nstd203human GRCh38 chr17: 34,963,853-34,963,870 , GRCh37.p13 chr17: 33,290,872-33,290,889 CCT6B, ZNF830
    nsv5029046copy number variation1nstd200human GRCh38 chr17: 34,959,348-34,982,808 , GRCh37.p13 chr17: 33,286,367-33,309,827 ZNF830, LIG3, 1 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675860copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,073,917-33,863,479 , GRCh38.p12 chr17: 34,746,898-35,536,460 RPL37P22, LIG3, 26 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
    nsv4436271copy number variation1nstd102humanUncertain significance GRCh37 chr17: 31,889,285-33,557,612 , GRCh38.p12 chr17: 33,562,266-35,230,593 LOC105371739, CCL7, 33 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
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4234046copy number variation1nstd166human GRCh37.p13 chr17: 30,657,307-33,838,598 , GRCh38.p12 chr17: 32,330,288-35,511,579 , PSMD11, 65 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
    nsv3907376copy number variation1nstd102humanUncertain significance GRCh37 chr17: 32,351,496-34,455,576 , GRCh38.p12 chr17: 34,024,477-35,919,248 CCL8, TAF5LP1, 67 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
    nsv3896751copy number variation1nstd102humanUncertain significance GRCh37 chr17: 32,654,402-33,353,332 , GRCh38.p12 chr17: 34,327,383-35,026,313 LIG3, OSTCP7, 12 more genes
    nsv3143488copy number variation1nstd151human GRCh37 chr17: 33,255,064-33,289,709 , GRCh38.p12 chr17: 34,928,045-34,962,690 ZNF830, CCT6B
    nsv1868761short tandem repeat2nstd128human GRCh37 chr17: 33,291,178-33,291,208 , GRCh38.p12 chr17: 34,964,159-34,964,189 ZNF830, CCT6B
    nsv1868091short tandem repeat1nstd128human GRCh37 chr17: 33,289,069-33,289,099 , GRCh38.p12 chr17: 34,962,050-34,962,080 ZNF830, CCT6B
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