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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062837inversion1nstd229human GRCh38 chr11: 40,841,838-44,720,409 , GRCh37.p13 chr11: 40,863,388-44,741,959 TTC17, ACCSL, 35 more genes
    nsv6916839copy number variation1nstd229human GRCh38 chr11: 43,266,619-43,268,780 , GRCh37.p13 chr11: 43,288,169-43,290,330 HNRNPKP3
    nsv6898399copy number variation1nstd229human GRCh38 chr11: 42,961,831-43,288,059 , GRCh37.p13 chr11: 42,983,381-43,309,609 HNRNPKP3, LOC100533710
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6315293copy number variation1nstd102humanUncertain significance GRCh38 chr11: 42,871,836-44,852,545 , GRCh37.p13 chr11: 42,893,386-44,874,096 ACCS, LINC02704, 26 more genes
    nsv6291196copy number variation1nstd102humanPathogenic GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167 LINC02687, ALKBH3, 86 more genes
    nsv6132366copy number variation1nstd213human GRCh37 chr11: 43,230,000-43,400,001 , GRCh38.p12 chr11: 43,208,450-43,378,451 API5, TTC17, 1 more genes
    nsv6132178copy number variation1nstd213human GRCh37 chr11: 42,590,000-43,350,001 , GRCh38.p12 chr11: 42,568,450-43,328,451 API5, HNRNPKP3, 1 more genes
    nsv6093619insertion1nstd212human GRCh38 chr11: 43,265,301-43,265,301 , GRCh37.p13 chr11: 43,286,851-43,286,851 HNRNPKP3
    nsv5970489insertion1nstd209human GRCh38 chr11: 43,265,300-43,265,300 , GRCh37.p13 chr11: 43,286,850-43,286,850 HNRNPKP3
    nsv5538932insertion1nstd206human GRCh38 chr11: 43,265,294-43,265,304 , GRCh37.p13 chr11: 43,286,844-43,286,854 HNRNPKP3
    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
    nsv4729468copy number variation1nstd102humanUncertain significance GRCh37 chr11: 43,223,479-44,266,544 , GRCh38.p12 chr11: 43,201,929-44,244,994 MIR670, ALKBH3, 18 more genes
    nsv4703289copy number variation1nstd195human GRCh37 chr11: 43,228,451-43,367,901 , GRCh38.p12 chr11: 43,206,901-43,346,351 API5, HNRNPKP3
    nsv3956054copy number variation1nstd168human GRCh38 chr11: 43,256,857-43,276,381 , GRCh37.p13 chr11: 43,278,407-43,297,931 HNRNPKP3
    nsv3931490insertion1nstd167human GRCh37 chr11: 43,286,825-43,286,825 , GRCh38.p12 chr11: 43,265,275-43,265,275 HNRNPKP3
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 F2, PSMC3, 140 more genes
    nsv3924016copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 40,666,800-44,162,262 , GRCh37 chr11: 40,710,224-44,205,686 , GRCh38 chr11: 40,688,674-44,184,136 EXT2, API5, 29 more genes
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