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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5286073copy number variation1nstd204human GRCh38.p13 chr17: 7,855,801-8,224,900 , GRCh37.p13 chr17: 7,759,119-8,128,218 , TRW-CCA3-3, 45 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729929copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,650,649-8,040,151 , GRCh38.p12 chr17: 6,747,330-8,136,833 CYB5D1, GPS2, 98 more genes
    nsv4683612copy number variation2nstd102humanUncertain significance GRCh37 chr17: 6,589,506-8,151,374 , GRCh38.p12 chr17: 6,686,187-8,248,056 ALOX12P2, DLG4, 124 more genes
    nsv4665896copy number variation1nstd186human GRCh37 chr17: 7,832,101-7,835,300 , GRCh38.p12 chr17: 7,928,783-7,931,982 KCNAB3, TRAPPC1, 1 more genes
    nsv4627642copy number variation1nstd183human GRCh37 chr17: 7,832,101-7,835,300 , GRCh38.p12 chr17: 7,928,783-7,931,982 KCNAB3, CNTROB, 1 more genes
    nsv4457674copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,676,383-8,350,870 , GRCh38.p12 chr17: 7,773,065-8,447,552 ARHGEF15, TRI-AAT4-1, 57 more genes
    nsv4453653copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,572,917-8,285,638 , GRCh38 chr17: 7,669,599-8,382,320 TRS-AGA2-6, ODF4, 59 more genes
    nsv4239367copy number variation1nstd166human GRCh37.p13 chr17: 7,828,000-7,839,000 , GRCh38.p12 chr17: 7,924,682-7,935,682 CNTROB, KCNAB3, 1 more genes
    nsv4235545copy number variation1nstd166human GRCh37.p13 chr17: 7,832,000-7,837,000 , GRCh38.p12 chr17: 7,928,682-7,933,682 TRAPPC1, KCNAB3, 1 more genes
    nsv4233738copy number variation1nstd166human GRCh37.p13 chr17: 7,827,572-7,858,803 , GRCh38.p12 chr17: 7,924,254-7,955,485 , KCNAB3, 2 more genes
    nsv3923531copy number variation1nstd102humanPathogenic NCBI36 chr17: 7,322,238-8,279,567 , GRCh37 chr17: 7,381,514-8,338,842 , GRCh38 chr17: 7,478,195-8,435,524 SLC25A35, TRP-CGG1-3, 82 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 PSMB6, RNU6-1065P, 409 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 KIF1C-AS1, TMEM107, 433 more genes
    nsv3911050copy number variation1nstd102humanPathogenic GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391 C17orf49, SPEM1, 209 more genes
    nsv3910343copy number variation1nstd102humanPathogenic GRCh37 chr17: 5,636,297-7,942,140 , NCBI36 chr17: 5,577,021-7,882,865 , GRCh38 chr17: 5,732,977-8,038,822 RPL23AP73, TNFSF13, 106 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
    nsv3904771copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115 SLC2A4, CCDC92B, 401 more genes
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