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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7075670inversion1nstd229human GRCh38 chr17: 4,410,937-4,527,721 , GRCh37.p13 chr17: 4,314,232-4,431,016 SPNS2, SPNS3, 1 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv7064614inversion1nstd229human GRCh38 chr17: 4,533,341-4,577,255 , GRCh37.p13 chr17: 4,436,636-4,480,550 TXNP4, MYBBP1A, 2 more genes
    nsv6997822copy number variation1nstd229human GRCh38 chr17: 4,360,080-4,526,090 , GRCh37.p13 chr17: 4,263,375-4,429,385 UBE2G1, SPNS2, 3 more genes
    nsv6997389copy number variation1nstd229human GRCh38 chr17: 4,494,740-4,553,307 , GRCh37.p13 chr17: 4,398,035-4,456,602 SPNS2-AS1, MYBBP1A, 1 more genes
    nsv6997184copy number variation1nstd229human GRCh38 chr17: 3,896,021-4,616,821 , GRCh37.p13 chr17: 3,799,315-4,520,116 RN7SL774P, LINC01996, 20 more genes
    nsv6997021copy number variation1nstd229human GRCh38 chr17: 4,499,946-4,499,973 , GRCh37.p13 chr17: 4,403,241-4,403,268 SPNS2
    nsv6995188copy number variation1nstd229human GRCh38 chr17: 4,499,804-4,499,869 , GRCh37.p13 chr17: 4,403,099-4,403,164 SPNS2
    nsv6994644copy number variation1nstd229human GRCh38 chr17: 4,522,849-4,539,100 , GRCh37.p13 chr17: 4,426,144-4,442,395 MYBBP1A, SPNS2
    nsv6993617copy number variation1nstd229human GRCh38 chr17: 4,537,275-4,655,788 , GRCh37.p13 chr17: 4,440,570-4,559,083 LOC105371498, SPNS2, 8 more genes
    nsv6992706copy number variation1nstd229human GRCh38 chr17: 4,530,293-4,579,802 , GRCh37.p13 chr17: 4,433,588-4,483,097 SPNS2, TXNP4, 2 more genes
    nsv6992465copy number variation1nstd229human GRCh38 chr17: 4,507,081-4,612,815 , GRCh37.p13 chr17: 4,410,376-4,516,110 SMTNL2, MYBBP1A, 4 more genes
    nsv6991212copy number variation1nstd229human GRCh38 chr17: 4,362,295-4,524,160 , GRCh37.p13 chr17: 4,265,590-4,427,455 RN7SL774P, SPNS2-AS1, 3 more genes
    nsv6990318copy number variation1nstd229human GRCh38 chr17: 4,539,372-4,539,559 , GRCh37.p13 chr17: 4,442,667-4,442,854 MYBBP1A, SPNS2
    nsv6989045copy number variation1nstd229human GRCh38 chr17: 4,533,301-4,587,400 , GRCh37.p13 chr17: 4,436,596-4,490,695 MYBBP1A, SMTNL2, 3 more genes
    nsv6988328copy number variation1nstd229human GRCh38 chr17: 4,518,275-4,555,248 , GRCh37.p13 chr17: 4,421,570-4,458,543 MYBBP1A, GGT6, 1 more genes
    nsv6987467copy number variation1nstd229human GRCh38 chr17: 4,431,604-4,611,542 , GRCh37.p13 chr17: 4,334,899-4,514,837 SPNS2, TXNP4, 6 more genes
    nsv6986972copy number variation1nstd229human GRCh38 chr17: 4,525,536-4,537,812 , GRCh37.p13 chr17: 4,428,831-4,441,107 MYBBP1A, SPNS2
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