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Items: 13

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    Number of Variants: 13

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5674221copy number variation1nstd102humanPathogenic GRCh38 chrMT: 6,468-15,586 , GRCh37 chrMT: 6,468-15,586 ATP8, ND5, 20 more genes
    nsv5674222copy number variation1nstd102humanPathogenic GRCh38 chrMT: 7,126-13,988 , GRCh37 chrMT: 7,126-13,988 ATP8, TRNH, 20 more genes
    nsv4685968copy number variation1nstd102humanPathogenic GRCh37 chrMT: 8,839-14,895 , GRCh38 chrMT: 8,839-14,895 ATP8, TRNG, 16 more genes
    nsv4685928copy number variation1nstd102humanPathogenic GRCh38 chrMT: 6,003-11,220 , GRCh37 chrMT: 6,003-11,220 ATP8, COX2, 21 more genes
    nsv4685910copy number variation1nstd102humanPathogenic GRCh37 chrMT: 8,350-13,450 , GRCh38 chrMT: 8,350-13,450 ATP8, TRNK, 15 more genes
    nsv5674153copy number variation2nstd102humannot provided, Pathogenic GRCh37 chrMT: 8,470-13,446 , GRCh38 chrMT: 8,470-13,446 ATP8, ND4, 15 more genes
    nsv4685954copy number variation1nstd102humanPathogenic GRCh38 chrMT: 8,480-13,440 , GRCh37 chrMT: 8,480-13,440 ATP8, COX2, 15 more genes
    nsv4685933copy number variation1nstd102humanPathogenic GRCh37 chrMT: 8,815-13,722 , GRCh38 chrMT: 8,815-13,722 ATP8, CYTB, 14 more genes
    nsv4685959copy number variation1nstd102humanPathogenic GRCh38 chrMT: 8,290-13,040 , GRCh37 chrMT: 8,290-13,040 ATP8, CYTB, 15 more genes
    nsv5674154copy number variation1nstd102humanPathogenic GRCh37 chrMT: 8,585-12,965 , GRCh38 chrMT: 8,585-12,965 ATP8, ATP6, 15 more genes
    nsv4685892copy number variation1nstd102humanPathogenic GRCh37 chrMT: 7,730-11,255 , GRCh38 chrMT: 7,730-11,255 ATP8, TRNG, 15 more genes
    nsv4685966copy number variation1nstd102humanLikely pathogenic GRCh37 chrMT: 5,794-14,876 , GRCh38 chrMT: 5,794-14,876 ATP8, ATP6, 26 more genes
    nsv4685879copy number variation1nstd102humanLikely pathogenic GRCh37 chrMT: 5,782-13,922 , GRCh38 chrMT: 5,782-13,922 ATP8, ATP6, 25 more genes
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