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Items: 1 to 20 of 390

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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
    nsv7076853inversion1nstd229human GRCh38 chr17: 75,625,589-75,630,077 , GRCh37.p13 chr17: 73,621,669-73,626,157 RECQL5, MYO15B
    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
    nsv7061272inversion1nstd229human GRCh38 chr17: 75,621,423-75,625,745 , GRCh37.p13 chr17: 73,617,503-73,621,825 RECQL5, MYO15B
    nsv6996686copy number variation1nstd229human GRCh38 chr17: 75,581,201-75,597,900 , GRCh37.p13 chr17: 73,577,282-73,593,981 MYO15B
    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
    nsv6993153copy number variation1nstd229human GRCh38 chr17: 75,624,301-75,627,600 , GRCh37.p13 chr17: 73,620,381-73,623,680 MYO15B, RECQL5
    nsv6992719copy number variation1nstd229human GRCh38 chr17: 75,594,801-75,597,000 , GRCh37.p13 chr17: 73,590,882-73,593,081 MYO15B
    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
    nsv6990004copy number variation1nstd229human GRCh38 chr17: 75,564,097-75,594,221 , GRCh37.p13 chr17: 73,560,178-73,590,302 LLGL2, MYO15B
    nsv6988143copy number variation1nstd229human GRCh38 chr17: 75,612,801-75,622,100 , GRCh37.p13 chr17: 73,608,882-73,618,180 MYO15B
    nsv6986244copy number variation1nstd229human GRCh38 chr17: 75,583,747-75,587,263 , GRCh37.p13 chr17: 73,579,828-73,583,344 MYO15B
    nsv6985955copy number variation1nstd229human GRCh38 chr17: 75,620,789-75,624,062 , GRCh37.p13 chr17: 73,616,869-73,620,142 MYO15B
    nsv6985134copy number variation1nstd229human GRCh38 chr17: 75,618,306-75,620,928 , GRCh37.p13 chr17: 73,614,386-73,617,008 MYO15B
    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
    nsv6978430copy number variation1nstd229human GRCh38 chr17: 75,556,874-75,623,475 , GRCh37.p13 chr17: 73,552,955-73,619,555 LLGL2, MYO15B
    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
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