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Items: 1 to 20 of 335

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7137196copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072 ECM1P2, LOC105378240, 482 more genes
    nsv7098818copy number variation1nstd102humanPathogenic GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956 LOC105374542, PPARGC1A, 232 more genes
    nsv7050627inversion1nstd229human GRCh38 chr4: 14,751,545-15,359,350 , GRCh37.p13 chr4: 14,753,169-15,360,974 LINC00504, RN7SKP170, 5 more genes
    nsv6732196copy number variation1nstd229human GRCh38 chr4: 15,007,624-15,007,919 , GRCh37.p13 chr4: 15,009,248-15,009,543 CPEB2, C1QTNF7-AS1
    nsv6731424copy number variation1nstd229human GRCh38 chr4: 15,064,523-15,064,579 , GRCh37.p13 chr4: 15,066,147-15,066,203 CPEB2, C1QTNF7-AS1
    nsv6727812copy number variation1nstd229human GRCh38 chr4: 14,993,541-15,026,099 , GRCh37.p13 chr4: 14,995,165-15,027,723 CPEB2, C1QTNF7-AS1, 1 more genes
    nsv6723127copy number variation1nstd229human GRCh38 chr4: 15,004,101-15,011,100 , GRCh37.p13 chr4: 15,005,725-15,012,724 C1QTNF7-AS1, CPEB2
    nsv6721682copy number variation1nstd229human GRCh38 chr4: 15,001,838-15,028,470 , GRCh37.p13 chr4: 15,003,462-15,030,094 C1QTNF7-AS1, CPEB2, 1 more genes
    nsv6720872copy number variation1nstd229human GRCh38 chr4: 15,026,185-15,026,218 , GRCh37.p13 chr4: 15,027,809-15,027,842 CPEB2, C1QTNF7-AS1
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6375424copy number variation1nstd223human GRCh38 chr4: 15,063,367-15,063,800 , GRCh37.p13 chr4: 15,064,991-15,065,424 C1QTNF7-AS1, CPEB2
    nsv6375275copy number variation1nstd223human GRCh38 chr4: 15,058,007-15,058,440 , GRCh37.p13 chr4: 15,059,631-15,060,064 CPEB2, C1QTNF7-AS1
    nsv6373771copy number variation1nstd223human GRCh38 chr4: 15,068,727-15,069,373 , GRCh37.p13 chr4: 15,070,351-15,070,997 CPEB2, C1QTNF7-AS1
    nsv6372667copy number variation1nstd223human GRCh38 chr4: 14,995,501-15,001,700 , GRCh37.p13 chr4: 14,997,125-15,003,324 CPEB2, CPEB2-DT
    nsv6371430copy number variation1nstd223human GRCh38 chr4: 15,012,301-15,013,300 , GRCh37.p13 chr4: 15,013,925-15,014,924 CPEB2, C1QTNF7-AS1
    nsv6367419copy number variation1nstd223human GRCh38 chr4: 15,023,293-15,023,774 , GRCh37.p13 chr4: 15,024,917-15,025,398 CPEB2, C1QTNF7-AS1
    nsv6367196copy number variation1nstd223human GRCh38 chr4: 15,066,901-15,069,700 , GRCh37.p13 chr4: 15,068,525-15,071,324 C1QTNF7-AS1, CPEB2
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