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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911215copy number variation1nstd209human GRCh38 chr7: 930,402-2,311,664 , GRCh37.p13 chr7: 970,038-2,351,299 , GPR146, 40 more genes
    nsv5909516copy number variation1nstd209human GRCh38 chr7: 1,059,547-1,059,698 , GRCh37.p13 chr7: 1,099,183-1,099,334 , C7orf50, 1 more genes
    nsv5846392copy number variation1nstd209human GRCh38 chr7: 1,046,991-1,047,990 , GRCh37.p13 chr7: 1,086,627-1,087,626 C7orf50, GPR146
    nsv5639268insertion1nstd207human GRCh38 chr7: 1,059,655-1,059,655 , GRCh37.p13 chr7: 1,099,291-1,099,291 , C7orf50, 1 more genes
    nsv5638242insertion1nstd207human GRCh38 chr7: 1,059,664-1,059,664 , GRCh37.p13 chr7: 1,099,300-1,099,300 , C7orf50, 1 more genes
    nsv5370086translocation1nstd200human GRCh38 chr7: 1,054,744-1,054,744 , GRCh38 chr7: 1,054,685-1,054,685 , GRCh37.p13 chr7: 1,094,321-1,094,321 , GRCh37.p13 chr7: 1,094,380-1,094,380 C7orf50, GPR146
    nsv5226601copy number variation1nstd204human GRCh38.p13 chr7: 909,101-1,222,900 , GRCh37.p13 chr7: 948,738-1,262,536 , ZFAND2A, 10 more genes
    nsv4759275insertion1nstd199human GRCh37 chr7: 1,099,277-1,099,277 , GRCh38.p12 chr7: 1,059,641-1,059,641 , C7orf50, 1 more genes
    nsv4735866copy number variation1nstd199human GRCh37 chr7: 1,099,277-1,099,488 , GRCh38.p12 chr7: 1,059,641-1,059,852 , C7orf50, 1 more genes
    nsv4729632copy number variation1nstd102humanUncertain significance GRCh37 chr7: 1,063,598-1,614,261 , GRCh38.p12 chr7: 1,023,962-1,574,625 MICALL2, INTS1, 14 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
    nsv4712990copy number variation1nstd195human GRCh37 chr7: 1,079,701-1,108,951 , GRCh38.p12 chr7: 1,040,065-1,069,315 , C7orf50, 1 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
    nsv4675062copy number variation1nstd102humanUncertain significance GRCh37 chr7: 1,065,860-1,812,800 , GRCh38.p12 chr7: 1,026,224-1,773,164 INTS1, MICALL2, 21 more genes
    nsv4663525copy number variation1nstd186human GRCh37 chr7: 1,098,611-1,099,591 , GRCh38.p12 chr7: 1,058,975-1,059,955 , C7orf50, 1 more genes
    nsv4605780copy number variation1nstd183human GRCh37 chr7: 1,098,611-1,099,591 , GRCh38.p12 chr7: 1,058,975-1,059,955 , GPR146, 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
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
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