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Items: 1 to 20 of 102

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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
    nsv4989067copy number variation1nstd200human GRCh38 chr11: 77,839,766-78,289,807 , GRCh37.p13 chr11: 77,550,812-78,000,853 KCTD21-AS1, NDUFC2, 13 more genes
    nsv4989064copy number variation1nstd200human GRCh38 chr11: 77,702,166-77,945,032 , GRCh37.p13 chr11: 77,413,211-77,656,078 FTH1P16, RSF1, 4 more genes
    nsv4842769copy number variation1nstd200human GRCh37 chr11: 77,550,812-78,000,853 , GRCh38.p12 chr11: 77,839,766-78,289,807 KCTD14, THRSP, 13 more genes
    nsv4729234copy number variation1nstd102humanUncertain significance GRCh37 chr11: 77,575,261-77,902,589 , GRCh38.p12 chr11: 77,864,215-78,191,543 LOC105369401, KCTD21, 12 more genes
    nsv4455314copy number variation2nstd102humanUncertain significance GRCh37 chr11: 77,410,575-77,785,783 , GRCh38.p12 chr11: 77,699,530-78,074,737 FTH1P16, AAMDC, 8 more genes
    nsv4209422copy number variation1nstd166human GRCh37.p13 chr11: 77,413,211-77,656,078 , GRCh38.p12 chr11: 77,702,166-77,945,032 FTH1P16, AAMDC, 4 more genes
    nsv4205200copy number variation1nstd166human GRCh37.p13 chr11: 77,578,380-77,578,436 , GRCh38.p12 chr11: 77,867,334-77,867,390 RPL21P95, AAMDC, 1 more genes
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 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
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
    nsv3894547copy number variation1nstd102humanUncertain significance GRCh37 chr11: 77,415,541-77,785,783 , GRCh38.p12 chr11: 77,704,496-78,074,737 AAMDC, NDUFC2, 8 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
    nsv3155022copy number variation1nstd151human GRCh37 chr11: 76,924,903-78,443,625 , GRCh38.p12 chr11: 77,213,858-78,732,580 USP35, LOC107984369, 33 more genes
    nsv3150202copy number variation1nstd151human GRCh37 chr11: 77,409,529-77,784,192 , GRCh38.p12 chr11: 77,698,484-78,073,146 AAMDC, INTS4, 8 more genes
    nsv3141458copy number variation1nstd151human GRCh37 chr11: 77,451,773-77,784,192 , GRCh38.p12 chr11: 77,740,728-78,073,146 NDUFC2, AAMDC, 7 more genes
    nsv3141157copy number variation1nstd151human GRCh37 chr11: 77,436,587-77,784,192 , GRCh38.p12 chr11: 77,725,542-78,073,146 NDUFC2-KCTD14, RPL21P95, 8 more genes
    esv4010871copy number variation1estd233human GRCh37 chr11: 77,537,000-77,620,000 , GRCh38.p12 chr11: 77,825,954-77,908,954 AAMDC, RSF1, 2 more genes
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