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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6308970copy number variation1nstd102humanPathogenic GRCh37 chr11: 2,187,460-2,191,953 , GRCh38.p12 chr11: 2,166,230-2,170,723 TH
    nsv6309758copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,310,735-55,313,868 , GRCh38.p12 chr14: 54,844,017-54,847,150 GCH1
    nsv6309759copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,312,466-55,313,868 , GRCh38.p12 chr14: 54,845,748-54,847,150 GCH1
    nsv7093843copy number variation1nstd102humanPathogenic GRCh37 chr11: 2,187,222-2,188,272 , GRCh38.p12 chr11: 2,165,992-2,167,042 TH
    nsv4682289copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,369,029-55,369,420 , GRCh38.p12 chr14: 54,902,311-54,902,702 GCH1
    nsv3884573copy number variation1nstd102humanPathogenic GRCh38 chr14: 54,902,301-54,902,683 , GRCh37 chr14: 55,369,019-55,369,401 GCH1
    nsv6309549copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,369,019-55,369,381 , GRCh38.p12 chr14: 54,902,301-54,902,663 GCH1
    nsv3888255copy number variation1nstd102humanPathogenic GRCh38 chr14: 54,865,307-54,865,456 , GRCh37 chr14: 55,332,025-55,332,174 GCH1
    nsv4449748copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,332,035-55,332,164 , GRCh38 chr14: 54,865,317-54,865,446 GCH1
    nsv5672575copy number variation1nstd102humanPathogenic GRCh37 chr14: 55,313,807-55,313,858 , GRCh38.p12 chr14: 54,847,089-54,847,140 GCH1
    nsv4682324copy number variation2nstd102humanLikely pathogenic GRCh37 chr11: 2,187,700-2,189,905 , GRCh38.p12 chr11: 2,166,470-2,168,675 TH
    nsv6957888copy number variation1nstd229human GRCh38 chr14: 54,866,746-54,874,679 , GRCh37.p13 chr14: 55,333,464-55,341,397 GCH1
    nsv6945529copy number variation1nstd229human GRCh38 chr14: 54,867,259-54,871,245 , GRCh37.p13 chr14: 55,333,977-55,337,963 GCH1
    nsv6949647copy number variation1nstd229human GRCh38 chr14: 54,847,056-54,850,553 , GRCh37.p13 chr14: 55,313,774-55,317,271 GCH1
    nsv6942766copy number variation1nstd229human GRCh38 chr14: 54,896,835-54,896,930 , GRCh37.p13 chr14: 55,363,553-55,363,648 GCH1
    nsv6490201copy number variation1nstd223human GRCh38 chr14: 54,897,532-54,900,108 , GRCh37.p13 chr14: 55,364,250-55,366,826 GCH1
    nsv6492608copy number variation1nstd223human GRCh38 chr14: 54,861,688-54,863,359 , GRCh37.p13 chr14: 55,328,406-55,330,077 GCH1
    nsv6476090copy number variation1nstd223human GRCh38 chr14: 54,851,953-54,853,127 , GRCh37.p13 chr14: 55,318,671-55,319,845 GCH1
    nsv5496707copy number variation1nstd206human GRCh38 chr14: 54,897,575-54,900,077 , GRCh37.p13 chr14: 55,364,293-55,366,795 GCH1
    nsv5497291copy number variation1nstd206human GRCh38 chr14: 54,861,688-54,863,358 , GRCh37.p13 chr14: 55,328,406-55,330,076 GCH1
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