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Items: 1 to 20 of 144

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6997924copy number variation1nstd229human GRCh38 chr17: 77,115,680-77,630,885 , GRCh37.p13 chr17: 75,111,762-75,626,967 SEPTIN9, LOC112268199, 11 more genes
    nsv6990287copy number variation1nstd229human GRCh38 chr17: 77,157,811-77,961,099 , GRCh37.p13 chr17: 75,153,893-75,957,181 LOC112268198, LOC107985079, 17 more genes
    nsv6987882copy number variation1nstd229human GRCh38 chr17: 77,245,545-77,603,685 , GRCh37.p13 chr17: 75,241,627-75,599,767 LOC112268198, SEPTIN9-DT, 7 more genes
    nsv6985284copy number variation1nstd229human GRCh38 chr17: 77,451,883-77,567,012 , GRCh37.p13 chr17: 75,447,965-75,563,094 LOC105371903, LOC100507351, 2 more genes
    nsv6984351copy number variation1nstd229human GRCh38 chr17: 77,526,301-77,540,400 , GRCh37.p13 chr17: 75,522,383-75,536,482 LOC400622
    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
    nsv6982239copy number variation1nstd229human GRCh38 chr17: 76,224,241-77,998,670 , GRCh37.p13 chr17: 74,220,322-75,994,751 MFSD11, PRPSAP1, 59 more genes
    nsv6980120copy number variation1nstd229human GRCh38 chr17: 77,515,587-77,525,092 , GRCh37.p13 chr17: 75,511,669-75,521,174 LOC400622
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6529914copy number variation1nstd223human GRCh38 chr17: 77,533,115-77,533,894 , GRCh37.p13 chr17: 75,529,197-75,529,976 LOC400622
    nsv6529225copy number variation1nstd223human GRCh38 chr17: 77,515,587-77,525,086 , GRCh37.p13 chr17: 75,511,669-75,521,168 LOC400622
    nsv6528208copy number variation1nstd223human GRCh38 chr17: 77,464,100-77,687,463 , GRCh37.p13 chr17: 75,460,182-75,683,545 LOC107985079, LOC100507351, 2 more genes
    nsv6522279copy number variation1nstd223human GRCh38 chr17: 77,451,883-77,567,012 , GRCh37.p13 chr17: 75,447,965-75,563,094 LOC400622, LOC105371903, 2 more genes
    nsv6519376copy number variation1nstd223human GRCh38 chr17: 77,115,680-77,630,882 , GRCh37.p13 chr17: 75,111,762-75,626,964 LOC105371903, CYCSP40, 11 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
    nsv5522277copy number variation1nstd206human GRCh38 chr17: 77,451,883-77,567,012 , GRCh37.p13 chr17: 75,447,965-75,563,094 SEPTIN9, LOC100507351, 2 more genes
    nsv5014052copy number variation1nstd200human GRCh38 chr17: 77,451,883-77,567,012 , GRCh37.p13 chr17: 75,447,965-75,563,094 LOC400622, SEPTIN9, 2 more genes
    nsv4854407copy number variation1nstd200human GRCh37 chr17: 75,447,965-75,563,094 , GRCh38.p12 chr17: 77,451,883-77,567,012 LOC400622, SEPTIN9, 2 more genes
    nsv4676341copy number variation1nstd102humanUncertain significance GRCh37 chr17: 74,509,193-75,602,123 , GRCh38.p12 chr17: 76,513,111-77,606,041 CYCSP40, RNU6-97P, 38 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
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