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Items: 1 to 20 of 177

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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
    nsv5275203copy number variation1nstd204human GRCh38.p13 chr11: 66,946,001-67,700,500 , GRCh37.p13 chr11: 66,713,472-67,467,971 , PC, 38 more genes
    nsv4985095copy number variation1nstd200human GRCh38 chr11: 67,578,495-67,641,726 , GRCh37.p13 chr11: 67,345,966-67,409,197 GSTP1, ACY3, 5 more genes
    nsv4985094copy number variation1nstd200human GRCh38 chr11: 67,577,565-67,989,543 , GRCh37.p13 chr11: 67,345,036-67,757,014 , RNU6-46P, 24 more genes
    nsv4979949copy number variation1nstd200human GRCh38 chr11: 67,635,649-67,642,855 , GRCh37.p13 chr11: 67,403,120-67,410,326 TBX10, ACY3
    nsv4847858copy number variation1nstd200human GRCh37 chr11: 67,345,007-67,757,088 , GRCh38.p12 chr11: 67,577,536-67,989,617 , LOC105369359, 24 more genes
    nsv4839345copy number variation1nstd200human GRCh37 chr11: 67,345,966-67,409,197 , GRCh38.p12 chr11: 67,578,495-67,641,726 GSTP1, ACY3, 5 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
    nsv4708748copy number variation1nstd195human GRCh37 chr11: 67,250,051-67,474,151 , GRCh38.p12 chr11: 67,482,580-67,706,680 AIP, ALDH3B2, 12 more genes
    nsv4675137copy number variation1nstd102humanUncertain significance GRCh37 chr11: 66,820,585-67,979,510 , GRCh38.p12 chr11: 67,053,114-68,212,043 PPP1CA, RPS3AP40, 58 more genes
    nsv4613845copy number variation1nstd183human GRCh37 chr11: 67,351,177-67,474,034 , GRCh38.p12 chr11: 67,583,706-67,706,563 ALDH3B2, GSTP1, 7 more genes
    nsv4607860copy number variation2nstd183human GRCh37 chr11: 67,358,348-67,762,604 , GRCh38.p12 chr11: 67,590,877-67,995,133 , OR7E145P, 23 more genes
    nsv4455772copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,081,259-67,471,729 , GRCh38.p12 chr11: 67,313,788-67,704,258 LOC100130987, RPL37P2, 27 more genes
    nsv4419282copy number variation1nstd174human GRCh37 chr11: 67,319,916-67,764,068 , GRCh38.p12 chr11: 67,552,445-67,996,597 , UNC93B1, 24 more genes
    nsv4381954copy number variation1nstd173human GRCh37 chr11: 67,360,797-67,799,144 , GRCh38.p12 chr11: 67,593,326-68,031,677 , ALDH3B2, 26 more genes
    nsv4369340copy number variation1nstd173human GRCh37 chr11: 67,349,006-67,404,726 , GRCh38.p12 chr11: 67,581,535-67,637,255 NUDT8, TBX10, 4 more genes
    nsv4366606copy number variation1nstd173human GRCh37 chr11: 67,349,587-67,799,144 , GRCh38.p12 chr11: 67,582,116-68,031,677 , NDUFS8, 27 more genes
    nsv4349000copy number variation1nstd102humanPathogenic GRCh37 chr11: 65,138,976-67,574,402 , GRCh38.p12 chr11: 65,371,505-67,806,931 SNORD13F, ZNRD2, 141 more genes
    nsv4209280copy number variation1nstd166human GRCh37.p13 chr11: 67,345,897-67,409,197 , GRCh38.p12 chr11: 67,578,426-67,641,726 GSTP1, NDUFV1, 5 more genes
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