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Items: 1 to 20 of 645

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076292inversion1nstd229human GRCh38 chr16: 55,747,536-55,828,986 , GRCh37.p13 chr16: 55,781,448-55,862,898 CES1P1, CES1P2, 1 more genes
    nsv7075398inversion1nstd229human GRCh38 chr16: 55,758,051-55,784,311 , GRCh37.p13 chr16: 55,791,963-55,818,223 CES1P1
    nsv7074555inversion1nstd229human GRCh38 chr16: 55,605,091-55,798,321 , GRCh37.p13 chr16: 55,639,003-55,832,233 SLC6A2, CES1P1, 2 more genes
    nsv7073745inversion1nstd229human GRCh38 chr16: 55,751,496-55,886,859 , GRCh37.p13 chr16: 55,785,408-55,920,771 CES1P1, CES5A, 1 more genes
    nsv7069987inversion1nstd229human GRCh38 chr16: 55,753,535-55,885,727 , GRCh37.p13 chr16: 55,787,447-55,919,639 CES5A, CES1, 1 more genes
    nsv7069046inversion1nstd229human GRCh38 chr16: 55,769,019-55,824,582 , GRCh37.p13 chr16: 55,802,931-55,858,494 CES1, CES1P1
    nsv7063904inversion1nstd229human GRCh38 chr16: 54,352,554-57,044,545 , GRCh37.p13 chr16: 54,386,466-57,078,457 LOC102725116, OGFOD1, 65 more genes
    nsv7063552inversion1nstd229human GRCh38 chr16: 55,770,661-55,776,915 , GRCh37.p13 chr16: 55,804,573-55,810,827 CES1P1
    nsv7062038inversion1nstd229human GRCh38 chr16: 55,762,489-55,831,110 , GRCh37.p13 chr16: 55,796,401-55,865,022 CES1P1, CES1
    nsv6988150copy number variation1nstd229human GRCh38 chr16: 55,483,186-56,126,631 , GRCh37.p13 chr16: 55,517,098-56,160,543 CES1P1, LOC105371280, 11 more genes
    nsv6987484copy number variation1nstd229human GRCh38 chr16: 55,765,801-55,788,700 , GRCh37.p13 chr16: 55,799,713-55,822,612 CES1P1
    nsv6637586copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,573-62,203,182 , GRCh38.p12 chr16: 46,469,661-62,169,278 LINC02140, LOC100130602, 279 more genes
    nsv6637389copy number variation1nstd102humanUncertain significance GRCh37 chr16: 55,723,839-56,330,832 , GRCh38.p12 chr16: 55,689,927-56,296,920 LOC107984815, MIR3935, 11 more genes
    nsv6589659inversion1nstd223human GRCh38 chr16: 55,760,563-55,833,133 , GRCh37.p13 chr16: 55,794,475-55,867,045 CES1, CES1P1
    nsv6587849inversion1nstd223human GRCh38 chr16: 55,764,978-55,828,704 , GRCh37.p13 chr16: 55,798,890-55,862,616 CES1, CES1P1
    nsv6586941inversion1nstd223human GRCh38 chr16: 55,762,607-55,831,110 , GRCh37.p13 chr16: 55,796,519-55,865,022 CES1P1, CES1
    nsv6583268inversion1nstd223human GRCh38 chr16: 55,773,104-55,820,777 , GRCh37.p13 chr16: 55,807,016-55,854,689 CES1P1, CES1
    nsv6583002inversion1nstd223human GRCh38 chr16: 55,754,226-55,839,537 , GRCh37.p13 chr16: 55,788,138-55,873,449 CES1P1, CES1
    nsv6576627inversion1nstd223human GRCh38 chr16: 55,762,535-55,831,162 , GRCh37.p13 chr16: 55,796,447-55,865,074 CES1P1, CES1
    nsv6576397inversion1nstd223human GRCh38 chr16: 55,751,494-55,886,859 , GRCh37.p13 chr16: 55,785,406-55,920,771 CES1, CES1P1, 1 more genes
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