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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
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv6912757copy number variation1nstd229human GRCh38 chr11: 66,793,001-68,121,500 , GRCh37.p13 chr11: 66,560,472-67,888,967 CHKA-DT, LOC107984341, 66 more genes
    nsv6909452copy number variation1nstd229human GRCh38 chr11: 67,391,601-67,508,800 , GRCh37.p13 chr11: 67,159,072-67,276,271 PPP1CA, TBC1D10C, 14 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6902108copy number variation1nstd229human GRCh38 chr11: 67,421,001-67,505,300 , GRCh37.p13 chr11: 67,188,472-67,272,771 PITPNM1, TMEM134, 9 more genes
    nsv6898634copy number variation1nstd229human GRCh38 chr11: 67,266,601-67,521,900 , GRCh37.p13 chr11: 67,034,072-67,289,371 GRK2, CARNS1, 21 more genes
    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
    nsv6132273copy number variation1nstd213human GRCh37 chr11: 67,200,000-67,280,001 , GRCh38.p12 chr11: 67,432,529-67,512,530 RPS6KB2, AIP, 8 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5711325mobile element insertion1nstd211human GRCh38 chr11: 67,506,540-67,506,540 , GRCh37.p13 chr11: 67,274,011-67,274,011 CDK2AP2
    nsv5543519insertion1nstd206human GRCh38 chr11: 67,506,540-67,506,582 , GRCh37.p13 chr11: 67,274,011-67,274,053 CDK2AP2
    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
    nsv5279549copy number variation1nstd204human GRCh38.p13 chr11: 67,318,601-67,507,600 , GRCh37.p13 chr11: 67,086,072-67,275,071 TMEM134, PTPRCAP, 17 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
    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
    nsv4616079copy number variation1nstd183human GRCh37 chr11: 67,271,616-67,275,925 , GRCh38.p12 chr11: 67,504,145-67,508,454 PITPNM1, CDK2AP2
    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
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