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Items: 1 to 20 of 157

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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
    nsv7061338inversion1nstd229human GRCh38 chr11: 67,487,357-67,493,071 , GRCh37.p13 chr11: 67,254,828-67,260,542 MIR6752, AIP, 1 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
    nsv6899280copy number variation1nstd229human GRCh38 chr11: 67,504,024-67,504,062 , GRCh37.p13 chr11: 67,271,495-67,271,533 PITPNM1
    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
    nsv6309378copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,254,459-67,258,464 , GRCh38.p12 chr11: 67,486,988-67,490,993 MIR6752, AIP, 1 more genes
    nsv6309231copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,250,630-67,258,464 , GRCh38.p12 chr11: 67,483,159-67,490,993 MIR6752, AIP, 1 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
    nsv6084950insertion1nstd212human GRCh38 chr11: 67,499,572-67,499,572 , GRCh37.p13 chr11: 67,267,043-67,267,043 PITPNM1
    nsv6029065copy number variation1nstd212human GRCh38 chr11: 67,491,552-67,491,620 , GRCh37.p13 chr11: 67,259,023-67,259,091 PITPNM1, AIP
    nsv5970884insertion1nstd209human GRCh38 chr11: 67,499,572-67,499,572 , GRCh37.p13 chr11: 67,267,043-67,267,043 PITPNM1
    nsv5649661insertion1nstd207human GRCh38 chr11: 67,499,572-67,499,572 , GRCh37.p13 chr11: 67,267,043-67,267,043 PITPNM1
    nsv5380890copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 67,250,360-67,258,464 , GRCh38.p12 chr11: 67,482,889-67,490,993 AIP, PITPNM1, 1 more genes
    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
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