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Items: 1 to 20 of 303

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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
    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
    nsv6993153copy number variation1nstd229human GRCh38 chr17: 75,624,301-75,627,600 , GRCh37.p13 chr17: 73,620,381-73,623,680 MYO15B, 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
    nsv6984330copy number variation1nstd229human GRCh38 chr17: 75,652,670-75,653,263 , GRCh37.p13 chr17: 73,648,750-73,649,343 LOC107985013, RECQL5
    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
    nsv6984174copy number variation1nstd229human GRCh38 chr17: 75,642,538-75,665,465 , GRCh37.p13 chr17: 73,638,618-73,661,545 SAP30BP, SMIM6, 2 more genes
    nsv6981419copy number variation1nstd229human GRCh38 chr17: 75,648,198-75,652,854 , GRCh37.p13 chr17: 73,644,278-73,648,934 RECQL5, LOC107985013, 1 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
    nsv6534322copy number variation1nstd223human GRCh38 chr17: 75,659,160-75,682,224 , GRCh37.p13 chr17: 73,655,240-73,678,304 RECQL5, LOC107985013, 1 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
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