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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914523copy number variation1nstd209human GRCh38 chr7: 1,082,244-1,085,824 , GRCh37.p13 chr7: 1,121,880-1,125,460 GPER1, C7orf50, 1 more genes
    nsv5911215copy number variation1nstd209human GRCh38 chr7: 930,402-2,311,664 , GRCh37.p13 chr7: 970,038-2,351,299 , GPR146, 40 more genes
    nsv5907595copy number variation1nstd209human GRCh38 chr7: 1,086,595-1,086,671 , GRCh37.p13 chr7: 1,126,231-1,126,307 GPER1, C7orf50
    nsv5845867copy number variation1nstd209human GRCh38 chr7: 1,082,201-1,085,800 , GRCh37.p13 chr7: 1,121,837-1,125,436 C7orf50, GPER1, 1 more genes
    nsv5640263insertion1nstd207human GRCh38 chr7: 1,089,920-1,089,920 , GRCh37.p13 chr7: 1,129,556-1,129,556 C7orf50, GPER1
    nsv5534293insertion1nstd206human GRCh38 chr7: 1,089,951-1,089,971 , GRCh37.p13 chr7: 1,129,587-1,129,607 GPER1, C7orf50
    nsv5226601copy number variation1nstd204human GRCh38.p13 chr7: 909,101-1,222,900 , GRCh37.p13 chr7: 948,738-1,262,536 , ZFAND2A, 10 more genes
    nsv5107225mobile element insertion1nstd203human GRCh38 chr7: 1,089,920-1,089,951 , GRCh37.p13 chr7: 1,129,556-1,129,587 GPER1, C7orf50
    nsv4949498copy number variation1nstd200human GRCh38 chr7: 1,089,571-1,107,500 , GRCh37.p13 chr7: 1,129,207-1,147,136 C7orf50, GPER1
    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
    nsv4708903copy number variation1nstd195human GRCh37 chr7: 1,109,851-1,167,251 , GRCh38.p12 chr7: 1,070,215-1,127,615 , GPER1, 3 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
    nsv4675619copy number variation1nstd102humanUncertain significance GRCh37 chr7: 1,108,122-1,812,800 , GRCh38.p12 chr7: 1,068,486-1,773,164 ELFN1, PSMG3, 20 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
    nsv4611451copy number variation1nstd183human GRCh37 chr7: 1,103,268-1,303,061 , GRCh38.p12 chr7: 1,063,632-1,263,425 , GPER1, 6 more genes
    nsv4553543insertion1nstd166human GRCh37.p13 chr7: 1,129,556-1,129,556 , GRCh38.p12 chr7: 1,089,920-1,089,920 GPER1, C7orf50
    nsv4545396insertion1nstd166human GRCh37.p13 chr7: 1,126,076-1,126,076 , GRCh38.p12 chr7: 1,086,440-1,086,440 C7orf50, GPER1
    nsv4456827copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,376-19,520,619 , GRCh38.p12 chr7: 43,376-19,480,996 MIR6836, EEF1A1P26, 277 more genes
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