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Items: 1 to 20 of 214

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5920823copy number variation1nstd209human GRCh38 chr8: 96,250,299-96,250,539 , GRCh37.p13 chr8: 97,262,527-97,262,767 MTERF3
    nsv5641806insertion2nstd207human GRCh38 chr8: 96,250,681-96,250,681 , GRCh37.p13 chr8: 97,262,909-97,262,909 MTERF3
    nsv5634873insertion1nstd207human GRCh38 chr8: 96,250,682-96,250,682 , GRCh37.p13 chr8: 97,262,910-97,262,910 MTERF3
    nsv5627230insertion1nstd207human GRCh38 chr8: 96,250,615-96,250,615 , GRCh37.p13 chr8: 97,262,843-97,262,843 MTERF3
    nsv5484981copy number variation1nstd206human GRCh38 chr8: 96,250,303-96,250,540 , GRCh37.p13 chr8: 97,262,531-97,262,768 MTERF3
    nsv5473920copy number variation1nstd206human GRCh38 chr8: 96,250,128-96,250,572 , GRCh37.p13 chr8: 97,262,356-97,262,800 MTERF3
    nsv5316073copy number variation1nstd204human GRCh38.p13 chr8: 96,250,303-96,250,540 , GRCh37.p13 chr8: 97,262,531-97,262,768 MTERF3
    nsv5108388mobile element insertion1nstd203human GRCh38 chr8: 96,251,636-96,251,648 , GRCh37.p13 chr8: 97,263,864-97,263,876 MTERF3
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4965632copy number variation1nstd200human GRCh38 chr8: 96,217,510-96,239,195 , GRCh37.p13 chr8: 97,229,738-97,251,423 UQCRB, UQCRB-AS1, 1 more genes
    nsv4961370copy number variation1nstd200human GRCh38 chr8: 96,253,783-96,253,908 , GRCh37.p13 chr8: 97,266,011-97,266,136 MTERF3
    nsv4961369copy number variation1nstd200human GRCh38 chr8: 96,238,002-96,241,038 , GRCh37.p13 chr8: 97,250,230-97,253,266 MTERF3, UQCRB-AS1
    nsv4829191copy number variation1nstd200human GRCh37 chr8: 97,229,738-97,251,423 , GRCh38.p12 chr8: 96,217,510-96,239,195 UQCRB, UQCRB-AS1, 1 more genes
    nsv4822532copy number variation1nstd200human GRCh37 chr8: 97,250,230-97,253,266 , GRCh38.p12 chr8: 96,238,002-96,241,038 MTERF3, UQCRB-AS1
    nsv4754846insertion1nstd199human GRCh37 chr8: 97,262,848-97,262,848 , GRCh38.p12 chr8: 96,250,620-96,250,620 MTERF3
    nsv4729502copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 95,803,280-97,802,022 , GRCh38.p12 chr8: 94,791,052-96,789,794 SDC2, UQCRB, 29 more genes
    nsv4674970copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 96,646,399-98,973,327 , GRCh38.p12 chr8: 95,634,171-97,961,099 MATN2, SDC2, 26 more genes
    nsv4608177copy number variation1nstd183human GRCh37 chr8: 97,262,970-97,263,424 , GRCh38.p12 chr8: 96,250,742-96,251,196 MTERF3
    nsv4578266copy number variation1nstd102humanPathogenic GRCh37 chr8: 97,154,645-98,155,535 , GRCh38.p12 chr8: 96,142,417-97,143,307 LOC105375652, LOC102724804, 10 more genes
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