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Items: 1 to 20 of 64

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7070030inversion1nstd229human GRCh38 chr11: 16,966,270-21,356,221 , GRCh37.p13 chr11: 16,987,817-21,377,767 DBX1, PRMT3, 93 more genes
    nsv7069673inversion1nstd229human GRCh38 chr11: 19,148,674-19,583,004 , GRCh37.p13 chr11: 19,170,221-19,604,551 RNA5SP335, CSRP3, 8 more genes
    nsv6912878copy number variation1nstd229human GRCh38 chr11: 19,226,049-19,889,512 , GRCh37.p13 chr11: 19,247,596-19,911,058 MIR4694, NAV2-AS4, 8 more genes
    nsv6911780copy number variation1nstd229human GRCh38 chr11: 19,358,091-20,660,220 , GRCh37.p13 chr11: 19,379,638-20,681,766 RNA5SP335, HMGB1P40, 14 more genes
    nsv6906158copy number variation1nstd229human GRCh38 chr11: 18,831,701-26,837,040 , GRCh37.p13 chr11: 18,853,248-26,858,587 HTATIP2, LINC02686, 68 more genes
    nsv6905060copy number variation1nstd229human GRCh38 chr11: 19,504,908-19,509,781 , GRCh37.p13 chr11: 19,526,455-19,531,328 NAV2-AS4, NAV2-AS5, 1 more genes
    nsv6590311inversion1nstd223human GRCh38 chr11: 16,144,251-19,584,623 , GRCh37.p13 chr11: 16,165,797-19,606,170 LDHC, GLTPP1, 85 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv5507673copy number variation1nstd206human GRCh38 chr11: 16,359,999-20,627,000 , GRCh37.p13 chr11: 16,381,545-20,648,546 , CSRP3, 102 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4675502copy number variation1nstd102humanPathogenic GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341 MRGPRX5P, LDHC, 171 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4456526copy number variation1nstd102humanUncertain significance GRCh37 chr11: 18,894,624-19,554,521 , GRCh38.p12 chr11: 18,873,077-19,532,974 MRGPRX11P, NAV2, 15 more genes
    nsv3921634copy number variation1nstd102humanUncertain significance NCBI36 chr11: 18,504,345-20,726,247 , GRCh38 chr11: 18,526,222-20,748,125 , GRCh37 chr11: 18,547,769-20,769,671 NELL1, UEVLD, 41 more genes
    nsv3919437copy number variation1nstd102humanPathogenic GRCh37 chr11: 17,926,636-19,696,051 , NCBI36 chr11: 17,883,212-19,652,627 , GRCh38 chr11: 17,905,089-19,674,505 CSRP3-AS1, ZDHHC13, 55 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3906221copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-31,995,219 , GRCh38.p12 chr11: 230,615-31,973,673 PCNAP4, LIN7C, 688 more genes
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