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Items: 1 to 20 of 2155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv4004668copy number variation1estd231human GRCh37 chr10: 10,493,409-10,493,732 , GRCh38.p12 chr10: 10,451,446-10,451,769 CELF2-DT
    esv4004669copy number variation1estd231human GRCh37 chr10: 10,708,535-10,708,852 , GRCh38.p12 chr10: 10,666,572-10,666,889 CELF2
    esv4008197copy number variation1estd231human GRCh37 chr10: 11,325,802-11,326,489 , GRCh38.p12 chr10: 11,283,839-11,284,526 CELF2
    nsv507539sequence alteration1nstd49human NCBI35 chr10: 11,386,658-11,392,658 , GRCh37.p13 chr10: 11,346,652-11,352,652 , GRCh38.p12 chr10: 11,304,689-11,310,689 CELF2
    nsv507538sequence alteration2nstd49human NCBI35 chr10: 10,736,247-10,742,247 , GRCh37.p13 chr10: 10,696,241-10,702,241 , GRCh38.p12 chr10: 10,654,278-10,660,278 CELF2
    nsv6894638copy number variation1nstd229human GRCh38 chr10: 10,881,284-10,917,599 , GRCh37.p13 chr10: 10,923,247-10,959,562 CELF2
    nsv6880212copy number variation1nstd229human GRCh38 chr10: 10,572,401-10,599,000 , GRCh37.p13 chr10: 10,614,364-10,640,963 CELF2
    nsv6895328copy number variation1nstd229human GRCh38 chr10: 10,572,387-10,598,964 , GRCh37.p13 chr10: 10,614,350-10,640,927 CELF2
    nsv6880259copy number variation1nstd229human GRCh38 chr10: 10,667,501-10,691,800 , GRCh37.p13 chr10: 10,709,464-10,733,763 CELF2
    nsv6881287copy number variation1nstd229human GRCh38 chr10: 10,848,619-10,871,340 , GRCh37.p13 chr10: 10,890,582-10,913,303 CELF2
    nsv6885214copy number variation1nstd229human GRCh38 chr10: 10,826,264-10,847,431 , GRCh37.p13 chr10: 10,868,227-10,889,394 CELF2
    nsv6889865copy number variation1nstd229human GRCh38 chr10: 10,812,666-10,828,330 , GRCh37.p13 chr10: 10,854,629-10,870,293 CELF2
    nsv6890773copy number variation1nstd229human GRCh38 chr10: 10,614,038-10,627,823 , GRCh37.p13 chr10: 10,656,001-10,669,786 CELF2
    nsv6885642copy number variation1nstd229human GRCh38 chr10: 11,036,702-11,047,059 , GRCh37.p13 chr10: 11,078,665-11,089,022 CELF2
    nsv6880760copy number variation1nstd229human GRCh38 chr10: 10,532,778-10,543,095 , GRCh37.p13 chr10: 10,574,741-10,585,058 CELF2
    nsv6880413copy number variation1nstd229human GRCh38 chr10: 10,898,201-10,908,500 , GRCh37.p13 chr10: 10,940,164-10,950,463 CELF2
    nsv6887694copy number variation1nstd229human GRCh38 chr10: 10,481,046-10,489,761 , GRCh37.p13 chr10: 10,523,009-10,531,724 CELF2
    nsv6882352copy number variation1nstd229human GRCh38 chr10: 10,418,196-10,426,906 , GRCh37.p13 chr10: 10,460,159-10,468,869 CELF2-DT
    nsv6888029copy number variation1nstd229human GRCh38 chr10: 10,550,722-10,558,850 , GRCh37.p13 chr10: 10,592,685-10,600,813 CELF2
    nsv6890809copy number variation1nstd229human GRCh38 chr10: 10,670,900-10,678,882 , GRCh37.p13 chr10: 10,712,863-10,720,845 CELF2
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