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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5132605mobile element insertion1nstd203human GRCh38 chr11: 45,653,031-45,653,045 , GRCh37.p13 chr11: 45,674,581-45,674,595 CHST1
    nsv4881598inversion1nstd200human GRCh37 chr11: 45,670,647-45,670,734 , GRCh38.p12 chr11: 45,649,097-45,649,184 CHST1
    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
    nsv4729649copy number variation1nstd102humanUncertain significance GRCh37 chr11: 44,266,593-46,123,796 , GRCh38.p12 chr11: 44,245,043-46,102,245 LOC105376654, PHF21A, 31 more genes
    nsv4617283copy number variation2nstd183human GRCh37 chr11: 45,685,695-45,687,403 , GRCh38.p12 chr11: 45,664,145-45,665,853 CHST1
    nsv4318984inversion1nstd166human GRCh37.p13 chr11: 45,670,648-45,670,733 , GRCh38.p12 chr11: 45,649,098-45,649,183 CHST1
    nsv4207753copy number variation1nstd166human GRCh37.p13 chr11: 45,687,237-45,687,357 , GRCh38.p12 chr11: 45,665,687-45,665,807 CHST1
    nsv4203985copy number variation1nstd166human GRCh37.p13 chr11: 45,680,217-45,692,119 , GRCh38.p12 chr11: 45,658,667-45,670,569 CHST1
    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
    nsv3922177copy number variation1nstd102humanPathogenic GRCh38 chr11: 35,663,578-46,959,820 , GRCh37 chr11: 35,685,126-46,981,371 , NCBI36 chr11: 35,641,702-46,937,947 MIR3160-2, LOC105376631, 122 more genes
    nsv3921841copy number variation1nstd102humanPathogenic NCBI36 chr11: 42,531,785-46,092,919 , GRCh37 chr11: 42,575,209-46,136,343 , GRCh38 chr11: 42,553,659-46,114,792 PEX16, LOC105376655, 51 more genes
    nsv3919271copy number variation1nstd102humanPathogenic GRCh38 chr11: 44,136,593-46,121,139 , NCBI36 chr11: 44,114,719-46,099,266 , GRCh37 chr11: 44,158,143-46,142,690 LOC105376646, ALX4, 31 more genes
    nsv3914563copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735 ACP2, ARHGAP1, 143 more genes
    nsv3913842copy number variation1nstd102humanPathogenic GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735 MIR3160-1, RPS20P26, 162 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
    nsv3907541copy number variation1nstd102humanUncertain significance GRCh37 chr11: 45,229,091-46,342,834 , GRCh38.p12 chr11: 45,207,540-46,321,284 FBLIM1P2, HMGN2P37, 24 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
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