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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5727779mobile element insertion1nstd211human GRCh38 chr10: 63,146,132-63,146,132 , GRCh37.p13 chr10: 64,905,892-64,905,892 NRBF2
    nsv5713446mobile element insertion1nstd211human GRCh38 chr10: 63,146,145-63,146,145 , GRCh37.p13 chr10: 64,905,905-64,905,905 NRBF2
    nsv5625104insertion1nstd207human GRCh38 chr10: 63,133,977-63,133,977 , GRCh37.p13 chr10: 64,893,737-64,893,737 NRBF2
    nsv5410127mobile element insertion1nstd206human GRCh38 chr10: 63,146,145-63,146,196 , GRCh37.p13 chr10: 64,905,905-64,905,956 NRBF2
    nsv5191205mobile element insertion1nstd203human GRCh38 chr10: 63,146,119-63,146,119 , GRCh37.p13 chr10: 64,905,879-64,905,879 NRBF2
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976041copy number variation1nstd200human GRCh38 chr10: 63,155,034-63,161,840 , GRCh37.p13 chr10: 64,914,794-64,921,600 NRBF2
    nsv4831370copy number variation1nstd200human GRCh37 chr10: 64,914,794-64,921,600 , GRCh38.p12 chr10: 63,155,034-63,161,840 NRBF2
    nsv4761766insertion1nstd199human GRCh37 chr10: 64,893,730-64,893,730 , GRCh38.p12 chr10: 63,133,970-63,133,970 NRBF2
    nsv4675455copy number variation1nstd102humanPathogenic GRCh37 chr10: 50,250,603-69,256,083 , GRCh38.p12 chr10: 45,931,517-67,496,325 MRLN, LOC102724778, 242 more genes
    nsv4675436copy number variation1nstd102humanPathogenic GRCh37 chr10: 56,031,210-65,660,398 , GRCh38.p12 chr10: 54,271,450-63,900,638 MRPL35P2, MIR1296, 77 more genes
    nsv4674969copy number variation1nstd102humanUncertain significance GRCh37 chr10: 62,191,184-65,348,431 , GRCh38.p12 chr10: 60,431,426-63,588,671 RNU6-543P, ARID5B, 33 more genes
    nsv4610242copy number variation1nstd183human GRCh37 chr10: 64,863,429-64,896,477 , GRCh38.p12 chr10: 63,103,669-63,136,717 LOC105378328, RNU6-543P, 1 more genes
    nsv4556499insertion1nstd166human GRCh37.p13 chr10: 64,900,204-64,900,204 , GRCh38.p12 chr10: 63,140,444-63,140,444 NRBF2
    nsv4546177insertion1nstd166human GRCh37.p13 chr10: 64,905,879-64,905,879 , GRCh38.p12 chr10: 63,146,119-63,146,119 NRBF2
    nsv4488628mobile element insertion1nstd166human GRCh37.p13 chr10: 64,905,892-64,905,892 , GRCh38.p12 chr10: 63,146,132-63,146,132 NRBF2
    nsv4482178mobile element insertion1nstd166human GRCh37.p13 chr10: 64,910,886-64,910,886 , GRCh38.p12 chr10: 63,151,126-63,151,126 NRBF2
    nsv4388253copy number variation1nstd173human GRCh37 chr10: 64,861,870-64,896,044 , GRCh38.p12 chr10: 63,102,110-63,136,284 LOC105378328, RNU6-543P, 1 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
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