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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7067935inversion1nstd229human GRCh38 chr17: 49,372,959-49,554,293 , GRCh37.p13 chr17: 47,450,321-47,631,655 PHB1, ZNF652-AS1, 6 more genes
    nsv7066099inversion1nstd229human GRCh38 chr17: 48,881,742-49,437,637 , GRCh37.p13 chr17: 46,959,104-47,514,999 B4GALNT2P1, EIF4EP2, 21 more genes
    nsv7058912inversion1nstd229human GRCh38 chr17: 49,401,510-49,404,331 , GRCh37.p13 chr17: 47,478,872-47,481,693 PHB1
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6637543copy number variation1nstd102humanUncertain significance GRCh37 chr17: 46,753,824-47,577,721 , GRCh38.p12 chr17: 48,676,462-49,500,359 CALCOCO2, SUMO2P17, 37 more genes
    nsv6097051insertion1nstd212human GRCh38 chr17: 49,403,014-49,403,014 , GRCh37.p13 chr17: 47,480,376-47,480,376 PHB1
    nsv5970537inversion1nstd209human GRCh38 chr17: 48,889,540-49,449,733 , GRCh37.p13 chr17: 46,966,902-47,527,095 , ATP5MC1, 23 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5374810translocation1nstd200human GRCh38 chr17: 10,495,761-10,495,761 , GRCh38 chr17: 49,404,835-49,404,835 , GRCh37.p13 chr17: 47,482,197-47,482,197 , GRCh37.p13 chr17: 10,399,078-10,399,078 MYH1, PHB1, 1 more genes
    nsv5026355copy number variation1nstd200human GRCh38 chr17: 49,413,980-49,414,152 , GRCh37.p13 chr17: 47,491,342-47,491,514 PHB1
    nsv4457643copy number variation1nstd102humanUncertain significance GRCh37 chr17: 46,899,690-47,540,874 , GRCh38.p12 chr17: 48,822,328-49,463,512 FLJ40194, IGF2BP1, 24 more genes
    nsv4338396sequence alteration1nstd166human GRCh37.p13 chr17: 46,959,103-47,527,096 , GRCh38.p12 chr17: 48,881,741-49,449,734 , IGF2BP1, 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
    nsv3970569copy number variation1nstd168human GRCh38 chr17: 49,388,802-49,439,399 , GRCh37.p13 chr17: 47,466,164-47,516,761 PHB1, EIF4EP2, 1 more genes
    nsv3921455copy number variation1nstd102humanPathogenic NCBI36 chr17: 44,793,516-45,701,800 , GRCh37 chr17: 47,438,517-48,346,801 , GRCh38 chr17: 49,361,155-50,269,440 DLX4, H1-9P, 32 more genes
    nsv3920056copy number variation1nstd102humanUncertain significance NCBI36 chr17: 43,882,989-44,985,282 , GRCh38 chr17: 48,450,628-49,552,921 , GRCh37 chr17: 46,527,990-47,630,283 ZNF652-AS1, RPS10P25, 55 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
    nsv3913486copy number variation1nstd102humanPathogenic GRCh38 chr17: 48,520,885-49,511,208 , NCBI36 chr17: 43,953,246-44,943,569 , GRCh37 chr17: 46,598,247-47,588,570 MIR6165, NGFR, 54 more genes
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