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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142839copy number variation1nstd232human GRCh37.p13 chr11: 67,049,028-67,049,118 , GRCh38.p12 chr11: 67,281,557-67,281,647 GRK2
    nsv7139911copy number variation1nstd232human GRCh37.p13 chr11: 67,052,659-67,052,755 , GRCh38.p12 chr11: 67,285,188-67,285,284 GRK2
    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
    nsv6913713copy number variation1nstd229human GRCh38 chr11: 67,266,401-67,465,100 , GRCh37.p13 chr11: 67,033,872-67,232,571 RNU6-1238P, TMEM134, 16 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
    nsv6907448copy number variation1nstd229human GRCh38 chr11: 67,273,925-67,277,052 , GRCh37.p13 chr11: 67,041,396-67,044,523 GRK2
    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
    nsv6901997copy number variation1nstd229human GRCh38 chr11: 67,266,840-67,272,458 , GRCh37.p13 chr11: 67,034,311-67,039,929 GRK2
    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
    nsv6470005copy number variation1nstd223human GRCh38 chr11: 67,266,838-67,272,455 , GRCh37.p13 chr11: 67,034,309-67,039,926 GRK2
    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
    nsv6248160mobile element insertion1nstd215human GRCh38 chr11: 67,274,522-67,274,522 , GRCh37.p13 chr11: 67,041,993-67,041,993 GRK2
    nsv6132185copy number variation1nstd213human GRCh37 chr11: 66,970,000-67,070,001 , GRCh38.p12 chr11: 67,202,529-67,302,530 GRK2, KDM2A, 2 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
    nsv5969980insertion1nstd209human GRCh38 chr11: 67,274,495-67,274,495 , GRCh37.p13 chr11: 67,041,966-67,041,966 GRK2
    nsv5712166mobile element insertion2nstd211human GRCh38 chr11: 67,274,522-67,274,522 , GRCh37.p13 chr11: 67,041,993-67,041,993 GRK2
    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
    nsv5137166mobile element insertion1nstd203human GRCh38 chr11: 67,274,522-67,274,522 , GRCh37.p13 chr11: 67,041,993-67,041,993 GRK2
    nsv5132421mobile element insertion1nstd203human GRCh38 chr11: 67,274,495-67,274,522 , GRCh37.p13 chr11: 67,041,966-67,041,993 GRK2
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