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Items: 1 to 20 of 124

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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
    nsv5013700copy number variation1nstd200human GRCh38 chr17: 41,277,005-41,430,685 , GRCh37.p13 chr17|NW_003315953.1: 16,589-119,548 , GRCh37.p13 chr17: 39,433,257-39,586,937 KRT37, LOC105371778, 11 more genes
    nsv4680071copy number variation1nstd189human GRCh37.p13 chr17: 39,432,725-40,293,644 , GRCh38.p12 chr17: 41,276,473-42,141,626 ACLY, CNP, 50 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
    nsv3918835copy number variation1nstd102humanLikely benign GRCh38 chr17: 40,927,571-41,313,858 , NCBI36 chr17: 36,337,349-36,723,636 , GRCh37 chr17: 39,083,823-39,470,110 KRTAP9-2, KRTAP3-3, 42 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
    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
    nsv3900530copy number variation1nstd102humanLikely benign GRCh37 chr17: 39,043,189-39,492,499 , GRCh38.p12 chr17|NW_003871091.1: 36,205-278,131 , GRCh38.p12 chr17: 40,886,937-41,336,247 KRTAP9-3, TBC1D3P7, 45 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
    nsv3165767copy number variation1nstd151human GRCh37 chr17: 39,382,904-39,507,024 , GRCh38.p12 chr17|NW_003871093.1: 1-69,109 , GRCh38.p12 chr17|NW_003871092.1: 1-70,136 , GRCh38.p12 chr17: 41,226,652-41,350,772 KRTAP17-1, LOC105371778, 13 more genes
    nsv3165200copy number variation1nstd151human GRCh37 chr17: 39,405,970-39,524,247 , GRCh38.p12 chr17: 41,249,718-41,367,995 , GRCh38.p12 chr17|NW_003315953.2: 72,266-133,151 KRT33A, TBC1D3P7, 11 more genes
    nsv3163916copy number variation1nstd151human GRCh37 chr17: 39,197,113-39,780,766 , GRCh38.p12 chr17: 41,040,861-41,624,514 KRT43P, KRTAP9-12P, 56 more genes
    nsv3163703copy number variation1nstd151human GRCh37 chr17: 39,421,628-39,524,247 , GRCh38.p12 chr17: 41,265,376-41,367,995 , GRCh38.p12 chr17|NW_003315953.2: 72,266-133,151 KRTAP9-11P, KRTAP9-7, 9 more genes
    nsv3162563copy number variation1nstd151human GRCh37 chr17: 39,114,850-39,503,226 , GRCh38.p12 chr17: 40,958,598-41,346,974 KRTAP1-1, KRTAP4-8, 43 more genes
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