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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3891104copy number variation1nstd102humanBenign GRCh37 chr17: 5,973,448-5,974,332 , GRCh38.p12 chr17: 6,070,128-6,071,012 WSCD1
    nsv3907609copy number variation1nstd102humanBenign GRCh37 chr17: 5,973,710-5,974,192 , GRCh38.p12 chr17: 6,070,390-6,070,872 WSCD1
    nsv3890931copy number variation1nstd102humanLikely benign GRCh37 chr17: 5,725,112-6,145,658 , GRCh38.p12 chr17: 5,821,792-6,242,338 WSCD1, LOC105371508, 2 more genes
    nsv6291595copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,783,282-6,054,342 , GRCh38.p12 chr17: 5,879,962-6,151,022 WSCD1, LOC105371508, 1 more genes
    nsv3917164copy number variation1nstd102humanUncertain significance NCBI36 chr17: 5,921,892-6,168,654 , GRCh37.p13 chr17: 5,981,168-6,227,930 , GRCh38.p12 chr17: 6,077,848-6,324,610 WSCD1, BTF3P14, 2 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 WSCD1, RPS4XP17, 289 more genes
    nsv3915884copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093 WSCD1, LOC105371592, 222 more genes
    nsv3923152copy number variation1nstd102humanPathogenic NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343 WSCD1, PSMB6, 133 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 WSCD1, RPL23AP73, 106 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 WSCD1, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 WSCD1, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 WSCD1, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 WSCD1, SMURF2, 2366 more genes
    nsv3897625copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420 WSCD1, GP1BA, 439 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 WSCD1, KIF1C-AS1, 433 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 WSCD1, PSMB6, 409 more genes
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 WSCD1, RFLNB, 401 more genes
    nsv3904771copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115 WSCD1, SLC2A4, 401 more genes
    nsv3917777copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-7,394,448 , GRCh38 chr17: 198,748-7,491,129 , NCBI36 chr17: 48,539-7,335,172 WSCD1, PAFAH1B1, 267 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 WSCD1, C17orf49, 209 more genes
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