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Items: 1 to 20 of 392

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3889648copy number variation1nstd102humanUncertain significance GRCh37 chrX: 110,974,966-110,980,986 , GRCh38.p12 chrX: 111,731,738-111,737,758 ALG13
    nsv7098493copy number variation1nstd102humanUncertain significance GRCh37 chrX: 110,973,603-110,973,828 , GRCh38.p12 chrX: 111,730,375-111,730,600 ALG13
    nsv7098216copy number variation1nstd102humanUncertain significance GRCh37 chrX: 110,924,427-111,003,247 , GRCh38.p12 chrX: 111,681,199-111,760,019 ALG13
    nsv7082434copy number variation1nstd229human GRCh38 chrX: 111,761,621-111,767,978 , GRCh37.p13 chrX: 111,004,849-111,011,206 ALG13
    nsv7082432copy number variation1nstd229human GRCh38 chrX: 111,742,360-111,742,995 , GRCh37.p13 chrX: 110,985,588-110,986,223 ALG13
    nsv5421645copy number variation1nstd206human GRCh38 chrX: 111,696,836-111,697,157 , GRCh37.p13 chrX: 110,940,064-110,940,385 ALG13
    nsv6107084copy number variation1nstd212human GRCh38 chrX: 111,721,107-111,721,265 , GRCh37.p13 chrX: 110,964,335-110,964,493 ALG13
    nsv6101031copy number variation1nstd212human GRCh38 chrX: 111,721,193-111,721,318 , GRCh37.p13 chrX: 110,964,421-110,964,546 ALG13
    nsv6108081copy number variation1nstd212human GRCh38 chrX: 111,719,295-111,719,366 , GRCh37.p13 chrX: 110,962,523-110,962,594 ALG13
    nsv6107175copy number variation1nstd212human GRCh38 chrX: 111,721,090-111,721,155 , GRCh37.p13 chrX: 110,964,318-110,964,383 ALG13
    nsv5670959copy number variation1nstd207human GRCh38 chrX: 111,721,071-111,721,262 , GRCh37.p13 chrX: 110,964,299-110,964,490 ALG13
    nsv5668093copy number variation1nstd207human GRCh38 chrX: 111,721,071-111,721,134 , GRCh37.p13 chrX: 110,964,299-110,964,362 ALG13
    nsv4449071copy number variation1nstd175human GRCh37 chrX: 110,964,299-110,964,363 , GRCh38.p12 chrX: 111,721,071-111,721,135 ALG13
    nsv3950184copy number variation1nstd167human GRCh37 chrX: 110,964,299-110,964,363 , GRCh38.p12 chrX: 111,721,071-111,721,135 ALG13
    nsv3403079copy number variation1nstd162human GRCh38 chrX: 111,721,072-111,721,327 , GRCh37.p13 chrX: 110,964,300-110,964,555 ALG13
    nsv2784458copy number variation3nstd132human NCBI36 chrX: 110,800,463-110,851,339 , GRCh37.p13 chrX: 110,913,807-110,964,683 , GRCh38.p12 chrX: 111,670,579-111,721,455 ALG13
    nsv1187521copy number variation226nstd112Neandertal, Denisova hominin, human GRCh37 chrX: 110,989,057-110,996,274 , GRCh38.p12 chrX: 111,745,829-111,753,046 ALG13
    esv3677318copy number variation1estd217human GRCh37 chrX: 110,964,299-110,964,716 , GRCh38.p12 chrX: 111,721,071-111,721,488 ALG13
    esv3574306copy number variation2estd212human GRCh37 chrX: 110,981,092-110,989,664 , GRCh38.p12 chrX: 111,737,864-111,746,436 ALG13
    esv3574307copy number variation1estd212human GRCh37 chrX: 110,981,092-110,989,510 , GRCh38.p12 chrX: 111,737,864-111,746,282 ALG13
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