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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912089copy number variation1nstd209human GRCh38 chr7: 973,620-973,915 , GRCh37.p13 chr7: 1,013,256-1,013,551 COX19
    nsv5911215copy number variation1nstd209human GRCh38 chr7: 930,402-2,311,664 , GRCh37.p13 chr7: 970,038-2,351,299 , GPR146, 40 more genes
    nsv5462393copy number variation1nstd206human GRCh38 chr7: 905,625-987,665 , GRCh37.p13 chr7: 945,262-1,027,301 COX19, C7orf50, 2 more genes
    nsv5232246copy number variation1nstd204human GRCh38.p13 chr7: 972,308-973,607 , GRCh37.p13 chr7: 1,011,944-1,013,243 COX19
    nsv5226601copy number variation1nstd204human GRCh38.p13 chr7: 909,101-1,222,900 , GRCh37.p13 chr7: 948,738-1,262,536 , ZFAND2A, 10 more genes
    nsv4953198copy number variation1nstd200human GRCh38 chr7: 906,479-969,569 , GRCh37.p13 chr7: 946,116-1,009,205 COX19, ADAP1
    nsv4949490copy number variation1nstd200human GRCh38 chr7: 973,425-982,498 , GRCh37.p13 chr7: 1,013,061-1,022,134 CYP2W1, C7orf50, 1 more genes
    nsv4949489copy number variation1nstd200human GRCh38 chr7: 973,456-978,324 , GRCh37.p13 chr7: 1,013,092-1,017,960 C7orf50, COX19
    nsv4949488copy number variation1nstd200human GRCh38 chr7: 970,038-986,293 , GRCh37.p13 chr7: 1,009,674-1,025,929 CYP2W1, COX19, 1 more genes
    nsv4949487copy number variation1nstd200human GRCh38 chr7: 951,816-964,166 , GRCh37.p13 chr7: 991,452-1,003,802 COX19, ADAP1
    nsv4818247copy number variation1nstd200human GRCh37 chr7: 1,009,674-1,025,929 , GRCh38.p12 chr7: 970,038-986,293 C7orf50, COX19, 1 more genes
    nsv4729496copy number variation1nstd102humanUncertain significance GRCh37 chr7: 967,185-1,781,553 , GRCh38.p12 chr7: 927,549-1,741,917 ZFAND2A, LOC105375124, 25 more genes
    nsv4713124copy number variation1nstd195human GRCh37 chr7: 973,951-1,029,401 , GRCh38.p12 chr7: 934,315-989,765 ADAP1, CYP2W1, 2 more genes
    nsv4675871copy number variation1nstd102humanPathogenic GRCh37 chr7: 44,935-1,750,797 , GRCh38.p12 chr7: 44,935-1,711,161 C7orf50, LOC105375123, 47 more genes
    nsv4675301copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-1,648,288 , GRCh38.p12 chr7: 43,360-1,608,652 LOC112267991, MICALL2, 42 more genes
    nsv4615731copy number variation1nstd183human GRCh37 chr7: 947,942-1,027,116 , GRCh38.p12 chr7: 908,305-987,480 ADAP1, C7orf50, 2 more genes
    nsv4612573copy number variation1nstd183human GRCh37 chr7: 1,011,877-1,018,229 , GRCh38.p12 chr7: 972,241-978,593 COX19, C7orf50
    nsv4609745copy number variation1nstd183human GRCh37 chr7: 1,004,523-1,054,517 , GRCh38.p12 chr7: 964,887-1,014,881 COX19, CYP2W1, 1 more genes
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
    nsv4456136copy number variation1nstd102humanPathogenic GRCh37 chr7: 36,616-4,298,168 , GRCh38.p12 chr7: 36,616-4,258,536 LOC442497, LFNG, 85 more genes
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