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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5868676copy number variation1nstd209human GRCh38 chr17: 75,405,161-75,411,928 , GRCh37.p13 chr17: 73,401,242-73,408,009 GRB2, MIR3678, 1 more genes
    nsv5293564copy number variation1nstd204human GRCh38.p13 chr17: 75,324,501-75,458,800 , GRCh37.p13 chr17: 73,320,582-73,454,881 MIR3678, RNU6-938P, 3 more genes
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5285175copy number variation1nstd204human GRCh38.p13 chr17: 75,213,501-75,463,000 , GRCh37.p13 chr17: 73,209,596-73,459,081 MIR3678, MIF4GD-DT, 9 more genes
    nsv5014010copy number variation1nstd200human GRCh38 chr17: 75,062,121-75,491,883 , GRCh37.p13 chr17: 73,058,216-73,487,964 NUP85, RNU6-938P, 17 more genes
    nsv4854385copy number variation1nstd200human GRCh37 chr17: 73,058,216-73,487,964 , GRCh38.p12 chr17: 75,062,121-75,491,883 LOC107985034, SUMO2, 17 more genes
    nsv4676207copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,218,219-73,443,987 , GRCh38.p12 chr17: 75,222,124-75,447,906 GGA3, TMEM94, 9 more genes
    nsv4676145copy number variation1nstd102humanUncertain significance GRCh37 chr17: 72,945,415-73,414,786 , GRCh38.p12 chr17: 74,949,320-75,418,705 MIF4GD-DT, NT5C, 27 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4628995copy number variation1nstd183human GRCh37 chr17: 73,217,773-73,774,243 , GRCh38.p12 chr17: 75,221,678-75,778,162 , LOC107985013, 23 more genes
    nsv4576559mobile element insertion1nstd166human GRCh37.p13 chr17: 73,400,301-73,400,301 , GRCh38.p12 chr17: 75,404,220-75,404,220 GRB2, MIR3678
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4457509copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,281,505-73,443,727 , GRCh38.p12 chr17: 75,285,424-75,447,646 GRB2, RPL36AP7, 4 more genes
    nsv4261505copy number variation1nstd166human GRCh37.p13 chr17: 73,400,158-73,400,235 , GRCh38.p12 chr17: 75,404,077-75,404,154 MIR3678, GRB2
    nsv4253909copy number variation1nstd166human GRCh37.p13 chr17: 73,394,915-73,409,617 , GRCh38.p12 chr17: 75,398,834-75,413,536 RNU6-938P, GRB2, 1 more genes
    nsv3972399copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942 AANAT, ACOX1, 243 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 LOC101928447, GRB2, 368 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
    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
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