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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7073965inversion1nstd229human GRCh38 chr17: 75,577,011-75,829,469 , GRCh37.p13 chr17: 73,573,092-73,825,550 UNK, SMIM5, 10 more genes
    nsv7062058inversion1nstd229human GRCh38 chr17: 75,576,996-75,829,470 , GRCh37.p13 chr17: 73,573,077-73,825,551 UNC13D, SMIM5, 10 more genes
    nsv6994443copy number variation1nstd229human GRCh38 chr17: 75,515,499-75,718,036 , GRCh37.p13 chr17: 73,511,580-73,714,116 CASKIN2, SAP30BP, 7 more genes
    nsv6994222copy number variation1nstd229human GRCh38 chr17: 75,628,476-75,637,042 , GRCh37.p13 chr17: 73,624,556-73,633,122 SMIM5, RECQL5
    nsv6990261copy number variation1nstd229human GRCh38 chr17: 75,544,101-75,660,900 , GRCh37.p13 chr17: 73,540,182-73,656,980 MYO15B, LLGL2, 4 more genes
    nsv6984412copy number variation1nstd229human GRCh38 chr17: 75,631,600-75,631,643 , GRCh37.p13 chr17: 73,627,680-73,627,723 RECQL5, SMIM5
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6978515copy number variation1nstd229human GRCh38 chr17: 75,603,532-75,635,477 , GRCh37.p13 chr17: 73,599,613-73,631,557 MYO15B, RECQL5, 1 more genes
    nsv6589966inversion1nstd223human GRCh38 chr17: 75,576,986-75,829,587 , GRCh37.p13 chr17: 73,573,067-73,825,668 RECQL5, MIR4738, 10 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6520781copy number variation1nstd223human GRCh38 chr17: 75,577,126-75,638,253 , GRCh37.p13 chr17: 73,573,207-73,634,333 MYO15B, RECQL5, 1 more genes
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 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
    nsv5285796copy number variation1nstd204human GRCh37.p13 chr17: 73,542,682-73,669,280 , GRCh38.p13 chr17: 75,546,601-75,673,200 LLGL2, RECQL5, 5 more genes
    nsv5282319copy number variation1nstd204human GRCh38.p13 chr17: 75,609,901-75,917,300 , GRCh37.p13 chr17: 73,605,982-73,913,381 ITGB4, TRIM65, 15 more genes
    nsv4854394copy number variation1nstd200human GRCh37 chr17: 73,511,580-73,714,116 , GRCh38.p12 chr17: 75,515,499-75,718,036 , CASKIN2, 8 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
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