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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098477copy number variation1nstd102humanPathogenic GRCh37 chr9: 94,485,944-95,527,026 , GRCh38.p12 chr9: 91,723,662-92,764,744 LINC00475, MTATP6P29, 30 more genes
    nsv6875641copy number variation1nstd229human GRCh38 chr9: 92,355,786-92,425,179 , GRCh37.p13 chr9: 95,118,068-95,187,461 CENPP, OMD, 1 more genes
    nsv6875175copy number variation1nstd229human GRCh38 chr9: 92,337,320-92,458,659 , GRCh37.p13 chr9: 95,099,602-95,220,941 ASPN, CENPP, 3 more genes
    nsv6871993copy number variation1nstd229human GRCh38 chr9: 92,364,249-92,536,252 , GRCh37.p13 chr9: 95,126,531-95,298,534 ECM2, OGN, 4 more genes
    nsv6871346copy number variation1nstd229human GRCh38 chr9: 92,392,301-92,486,600 , GRCh37.p13 chr9: 95,154,583-95,248,882 ASPN, CENPP, 2 more genes
    nsv6870811copy number variation1nstd229human GRCh38 chr9: 92,418,261-92,428,806 , GRCh37.p13 chr9: 95,180,543-95,191,088 OMD, CENPP
    nsv6870680copy number variation1nstd229human GRCh38 chr9: 92,418,518-92,422,284 , GRCh37.p13 chr9: 95,180,800-95,184,566 OMD, CENPP
    nsv6870487copy number variation1nstd229human GRCh38 chr9: 91,906,361-92,583,443 , GRCh37.p13 chr9: 94,668,643-95,345,725 ROR2, LOC100420779, 25 more genes
    nsv6869562copy number variation1nstd229human GRCh38 chr9: 92,415,436-92,472,304 , GRCh37.p13 chr9: 95,177,718-95,234,586 OMD, CENPP, 1 more genes
    nsv6868620copy number variation1nstd229human GRCh38 chr9: 92,417,715-92,423,906 , GRCh37.p13 chr9: 95,179,997-95,186,188 CENPP, OMD
    nsv6864166copy number variation1nstd229human GRCh38 chr9: 92,421,552-92,449,804 , GRCh37.p13 chr9: 95,183,834-95,212,086 CENPP, OMD
    nsv6862088copy number variation1nstd229human GRCh38 chr9: 92,421,896-92,429,667 , GRCh37.p13 chr9: 95,184,178-95,191,949 OMD, CENPP
    nsv6861709copy number variation1nstd229human GRCh38 chr9: 92,397,991-92,439,830 , GRCh37.p13 chr9: 95,160,273-95,202,112 CENPP, OGN, 1 more genes
    nsv6860307copy number variation1nstd229human GRCh38 chr9: 92,418,264-92,428,806 , GRCh37.p13 chr9: 95,180,546-95,191,088 CENPP, OMD
    nsv6858480copy number variation1nstd229human GRCh38 chr9: 92,424,639-92,429,427 , GRCh37.p13 chr9: 95,186,921-95,191,709 OMD, CENPP
    nsv6638032copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,076,710-95,263,214 , GRCh38.p12 chr9: 92,314,428-92,500,932 OMD, CENPP, 5 more genes
    nsv6637685copy number variation1nstd102humanUncertain significance GRCh37 chr9: 94,666,958-95,339,157 , GRCh38.p12 chr9: 91,904,676-92,576,875 ECM2, IARS1, 25 more genes
    nsv6637423copy number variation1nstd102humanUncertain significance GRCh37 chr9: 95,079,794-95,503,060 , GRCh38.p12 chr9: 92,317,512-92,740,778 IPPK, LOC100420779, 11 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633498copy number variation1nstd224human GRCh37 chr9: 95,094,474-95,179,836 , GRCh38.p12 chr9: 92,332,192-92,417,554 OMD, CENPP, 2 more genes
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