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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098686copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 78,187,758-78,197,406 , GRCh38 chr11: 78,476,712-78,486,360 NARS2, LOC105369403
    nsv7093484insertion1nstd102humanUncertain significance GRCh37 chr11: 78,285,384-78,285,384 , GRCh38 chr11: 78,574,339-78,574,339 NARS2
    nsv7069675inversion1nstd229human GRCh38 chr11: 78,531,541-78,545,367 , GRCh37.p13 chr11: 78,242,587-78,256,413 LOC101928896, NARS2
    nsv7066286inversion1nstd229human GRCh38 chr11: 78,556,501-78,573,229 , GRCh37.p13 chr11: 78,267,547-78,284,274 NARS2, LOC101928896
    nsv7058775inversion1nstd229human GRCh38 chr11: 78,228,684-78,557,765 , GRCh37.p13 chr11: 77,939,730-78,268,811 ZNF75CP, LOC101928896, 5 more genes
    nsv6917400copy number variation1nstd229human GRCh38 chr11: 78,558,401-78,565,000 , GRCh37.p13 chr11: 78,269,447-78,276,046 LOC101928896, NARS2
    nsv6915240copy number variation1nstd229human GRCh38 chr11: 78,463,861-78,470,522 , GRCh37.p13 chr11: 78,174,907-78,181,568 NARS2, LOC105369403
    nsv6914930copy number variation1nstd229human GRCh38 chr11: 78,482,201-78,486,200 , GRCh37.p13 chr11: 78,193,247-78,197,246 LOC105369403, NARS2
    nsv6914891copy number variation1nstd229human GRCh38 chr11: 78,476,301-78,486,400 , GRCh37.p13 chr11: 78,187,347-78,197,446 NARS2, LOC105369403
    nsv6914686copy number variation1nstd229human GRCh38 chr11: 78,526,432-78,612,810 , GRCh37.p13 chr11: 78,237,478-78,323,855 LOC101928896, RNU6-311P, 2 more genes
    nsv6913918copy number variation1nstd229human GRCh38 chr11: 78,476,525-78,486,360 , GRCh37.p13 chr11: 78,187,571-78,197,406 NARS2, LOC105369403
    nsv6911141copy number variation1nstd229human GRCh38 chr11: 78,493,258-78,503,915 , GRCh37.p13 chr11: 78,204,304-78,214,961 LOC105369403, NARS2
    nsv6910015copy number variation1nstd229human GRCh38 chr11: 78,541,621-78,544,719 , GRCh37.p13 chr11: 78,252,667-78,255,765 NARS2, LOC101928896
    nsv6909682copy number variation1nstd229human GRCh38 chr11: 78,509,035-78,509,794 , GRCh37.p13 chr11: 78,220,081-78,220,840 NARS2
    nsv6907854copy number variation1nstd229human GRCh38 chr11: 78,548,351-78,548,381 , GRCh37.p13 chr11: 78,259,397-78,259,427 NARS2, LOC101928896
    nsv6907240copy number variation1nstd229human GRCh38 chr11: 78,459,191-78,459,547 , GRCh37.p13 chr11: 78,170,237-78,170,593 NARS2
    nsv6906723copy number variation1nstd229human GRCh38 chr11: 78,503,358-78,503,390 , GRCh37.p13 chr11: 78,214,404-78,214,436 NARS2
    nsv6906049copy number variation1nstd229human GRCh38 chr11: 78,476,714-78,486,361 , GRCh37.p13 chr11: 78,187,760-78,197,407 NARS2, LOC105369403
    nsv6905442copy number variation1nstd229human GRCh38 chr11: 78,509,866-78,516,150 , GRCh37.p13 chr11: 78,220,912-78,227,196 NARS2
    nsv6903782copy number variation1nstd229human GRCh38 chr11: 78,530,045-78,530,249 , GRCh37.p13 chr11: 78,241,091-78,241,295 NARS2
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