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Items: 1 to 20 of 118

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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
    nsv6915134copy number variation1nstd229human GRCh38 chr11: 20,381,001-20,467,200 , GRCh37.p13 chr11: 20,402,547-20,488,746 PRMT3, HTATIP2
    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
    nsv6637479copy number variation1nstd102humanUncertain significance GRCh37 chr11: 20,191,503-20,412,738 , GRCh38.p12 chr11: 20,169,957-20,391,192 HTATIP2, LOC105376583, 1 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
    nsv6275358copy number variation1nstd214human GRCh38 chr11: 20,361,887-20,361,948 , GRCh37.p13 chr11: 20,383,433-20,383,494 HTATIP2
    nsv6131919copy number variation1nstd213human GRCh37 chr11: 20,300,000-20,520,001 , GRCh38.p12 chr11: 20,278,454-20,498,455 PRMT3, HTATIP2
    nsv5923551copy number variation1nstd209human GRCh38 chr11: 20,096,010-20,731,492 , GRCh37.p13 chr11: 20,117,556-20,753,038 , HMGB1P40, 9 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
    nsv5505604copy number variation1nstd206human GRCh38 chr11: 20,372,111-20,372,194 , GRCh37.p13 chr11: 20,393,657-20,393,740 HTATIP2
    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
    nsv5345624translocation1nstd200human GRCh37 chr11: 20,393,657-20,393,657 , GRCh37 chr11: 20,393,740-20,393,740 , GRCh38.p12 chr11: 20,372,111-20,372,111 , GRCh38.p12 chr11: 20,372,194-20,372,194 HTATIP2
    nsv4984252copy number variation1nstd200human GRCh38 chr11: 20,159,358-20,476,084 , GRCh37.p13 chr11: 20,180,904-20,497,630 LOC105376583, DBX1, 2 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
    nsv4201794copy number variation1nstd166human GRCh37.p13 chr11: 20,393,657-20,393,740 , GRCh38.p12 chr11: 20,372,111-20,372,194 HTATIP2
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