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Items: 1 to 20 of 177

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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
    nsv5381106copy number variation1nstd102humanUncertain significance GRCh37 chr17: 45,297,260-45,300,418 , GRCh38.p12 chr17: 47,219,894-47,223,052 MYL4
    nsv5194716mobile element insertion1nstd203human GRCh38 chr17: 47,218,100-47,218,115 , GRCh37.p13 chr17: 45,295,466-45,295,481 MYL4
    nsv5016612copy number variation1nstd200human GRCh38 chr17: 47,211,981-47,217,755 , GRCh37.p13 chr17: 45,289,347-45,295,121 MYL4
    nsv4502065mobile element insertion1nstd166human GRCh37.p13 chr17: 45,295,565-45,295,565 , GRCh38.p12 chr17: 47,218,199-47,218,199 MYL4
    nsv4436018complex substitution1nstd102humanUncertain significance GRCh37 chr17: 45,008,570-45,994,044 , GRCh38.p12 chr17: 46,931,204-47,916,678 CDC27, ITGB3, 30 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
    nsv4271572copy number variation1nstd166human GRCh37.p13 chr17: 45,278,063-45,314,386 , GRCh38.p12 chr17: 47,200,697-47,237,020 MYL4
    nsv4255183copy number variation1nstd166human GRCh37.p13 chr17: 44,957,094-45,748,956 , GRCh38.p12 chr17: 46,879,728-47,671,590 MRPL45P2, KPNB1, 24 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
    nsv3165046copy number variation1nstd151human GRCh37 chr17: 45,287,027-45,300,413 , GRCh38.p12 chr17: 47,209,661-47,223,047 MYL4
    nsv3158534copy number variation1nstd151human GRCh37 chr17: 45,299,045-45,507,335 , GRCh38.p12 chr17: 47,221,679-47,429,969 NFE2L3P2, ITGB3, 6 more genes
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