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Items: 1 to 20 of 337

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148265copy number variation1nstd102humanPathogenic GRCh38 chr5: 176,447,531-177,312,407 , GRCh37.p13 chr5: 175,874,532-176,739,408 MXD3, FAF2, 19 more genes
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7057944inversion1nstd229human GRCh38 chr5: 172,134,356-176,589,266 , GRCh37.p13 chr5: 171,561,360-176,016,267 MIR10523, NIFKP2, 92 more genes
    nsv7050002inversion1nstd229human GRCh38 chr5: 175,906,338-177,936,522 , GRCh37.p13 chr5: 175,333,341-177,363,523 PRR7, OR1X5P, 60 more genes
    nsv7041901inversion1nstd229human GRCh38 chr5: 175,920,087-179,128,938 , GRCh37.p13 chr5: 175,347,090-178,555,939 LOC100288803, NHP2, 98 more genes
    nsv7040659inversion1nstd229human GRCh38 chr5: 174,927,732-178,443,561 , GRCh37.p13 chr5: 174,354,735-177,870,562 RN7SKP148, FAM193B-DT, 90 more genes
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6796459copy number variation1nstd229human GRCh38 chr5: 176,461,212-176,465,456 , GRCh37.p13 chr5: 175,888,213-175,892,457 FAF2
    nsv6789925copy number variation1nstd229human GRCh38 chr5: 176,467,945-176,478,470 , GRCh37.p13 chr5: 175,894,946-175,905,471 FAF2
    nsv6788079copy number variation1nstd229human GRCh38 chr5: 176,510,500-176,514,845 , GRCh37.p13 chr5: 175,937,501-175,941,846 FAF2
    nsv6784188copy number variation1nstd229human GRCh38 chr5: 176,469,355-176,474,851 , GRCh37.p13 chr5: 175,896,356-175,901,852 FAF2
    nsv6782309copy number variation1nstd229human GRCh38 chr5: 176,429,064-176,447,921 , GRCh37.p13 chr5: 175,856,065-175,874,922 FAF2
    nsv6782238copy number variation1nstd229human GRCh38 chr5: 176,459,802-176,475,149 , GRCh37.p13 chr5: 175,886,803-175,902,150 FAF2
    nsv6778832copy number variation1nstd229human GRCh38 chr5: 176,464,191-176,512,582 , GRCh37.p13 chr5: 175,891,192-175,939,583 FAF2
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6315318copy number variation1nstd102humanPathogenic GRCh38 chr5: 176,449,583-177,376,826 , GRCh37.p13 chr5: 175,876,584-176,803,827 FAF2, FGFR4, 22 more genes
    nsv6295211copy number variation1nstd186human GRCh37 chr5: 175,931,917-175,932,246 , GRCh38.p12 chr5: 176,504,916-176,505,245 FAF2
    nsv6291140copy number variation1nstd102humanUncertain significance GRCh37 chr5: 175,668,563-176,182,615 , GRCh38.p12 chr5: 176,241,560-176,755,614 MIR4281, HIGD2A, 16 more genes
    nsv6137542translocation1nstd213human GRCh37 chr5: 172,602,961-172,602,961 , GRCh37 chr5: 175,933,072-175,933,072 , GRCh38.p12 chr5: 173,175,958-173,175,958 , GRCh38.p12 chr5: 176,506,071-176,506,071 FAF2
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