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Items: 1 to 20 of 193

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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
    nsv7094010copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,250,630-67,250,738 , GRCh38.p12 chr11: 67,483,159-67,483,267 AIP
    nsv7094009copy number variation1nstd102humanPathogenic GRCh37 chr11: 67,250,360-67,250,738 , GRCh38.p12 chr11: 67,482,889-67,483,267 AIP
    nsv7061338inversion1nstd229human GRCh38 chr11: 67,487,357-67,493,071 , GRCh37.p13 chr11: 67,254,828-67,260,542 MIR6752, AIP, 1 more genes
    nsv6914194copy number variation1nstd229human GRCh38 chr11: 67,463,371-67,468,215 , GRCh37.p13 chr11: 67,230,842-67,235,686 AIP, TMEM134
    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
    nsv6908791copy number variation1nstd229human GRCh38 chr11: 67,472,561-67,478,649 , GRCh37.p13 chr11: 67,240,032-67,246,120 AIP
    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
    nsv6475229copy number variation1nstd223human GRCh38 chr11: 67,484,151-67,485,980 , GRCh37.p13 chr11: 67,251,622-67,253,451 AIP
    nsv6468683copy number variation1nstd223human GRCh38 chr11: 67,478,739-67,480,921 , GRCh37.p13 chr11: 67,246,210-67,248,392 AIP
    nsv6463399copy number variation1nstd223human GRCh38 chr11: 67,475,687-67,481,392 , GRCh37.p13 chr11: 67,243,158-67,248,863 AIP
    nsv6459014copy number variation1nstd223human GRCh38 chr11: 67,466,493-67,467,824 , GRCh37.p13 chr11: 67,233,964-67,235,295 TMEM134, AIP
    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
    nsv6309445copy number variation1nstd102humanPathogenic GRCh37 chr11: 67,250,360-67,254,666 , GRCh38.p12 chr11: 67,482,889-67,487,195 AIP
    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
    nsv6302945copy number variation1nstd186human GRCh37 chr11: 67,246,221-67,248,392 , GRCh38.p12 chr11: 67,478,750-67,480,921 AIP
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