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Items: 1 to 20 of 466

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147594copy number variation1nstd232human GRCh37.p13 chr5: 175,732,715-175,732,812 , GRCh38.p12 chr5: 176,305,712-176,305,809 SIMC1
    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
    nsv7056017inversion1nstd229human GRCh38 chr5: 176,261,208-176,261,562 , GRCh37.p13 chr5: 175,688,211-175,688,565 SIMC1
    nsv7055309inversion1nstd229human GRCh38 chr5: 176,251,563-176,434,793 , GRCh37.p13 chr5: 175,678,566-175,861,794 KIAA1191, BRCC3P1, 6 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
    nsv7046501inversion1nstd229human GRCh38 chr5: 176,329,593-176,329,638 , GRCh37.p13 chr5: 175,756,596-175,756,641 SIMC1
    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
    nsv7039242inversion1nstd229human GRCh38 chr5: 176,263,065-176,263,117 , GRCh37.p13 chr5: 175,690,068-175,690,120 SIMC1
    nsv7038290inversion1nstd229human GRCh38 chr5: 172,489,078-179,485,008 , GRCh37.p13 chr5: 171,916,082-178,912,009 ZFP2, NHP2, 168 more genes
    nsv6796184copy number variation1nstd229human GRCh38 chr5: 176,301,557-176,358,460 , GRCh37.p13 chr5: 175,728,560-175,785,463 KIAA1191, BRCC3P1, 1 more genes
    nsv6792578copy number variation1nstd229human GRCh38 chr5: 176,332,726-176,351,153 , GRCh37.p13 chr5: 175,759,729-175,778,156 KIAA1191, SIMC1
    nsv6792289copy number variation1nstd229human GRCh38 chr5: 176,273,701-176,276,300 , GRCh37.p13 chr5: 175,700,704-175,703,303 SIMC1
    nsv6792019copy number variation1nstd229human GRCh38 chr5: 176,290,381-176,290,421 , GRCh37.p13 chr5: 175,717,384-175,717,424 SIMC1
    nsv6790785copy number variation1nstd229human GRCh38 chr5: 176,168,901-176,342,000 , GRCh37.p13 chr5: 175,595,904-175,769,003 CEP192P1, LOC107986487, 2 more genes
    nsv6790585copy number variation1nstd229human GRCh38 chr5: 176,320,801-176,328,000 , GRCh37.p13 chr5: 175,747,804-175,755,003 SIMC1
    nsv6790116copy number variation1nstd229human GRCh38 chr5: 176,327,148-176,327,246 , GRCh37.p13 chr5: 175,754,151-175,754,249 SIMC1
    nsv6789869copy number variation1nstd229human GRCh38 chr5: 176,246,401-176,249,700 , GRCh37.p13 chr5: 175,673,404-175,676,703 SIMC1
    nsv6788973copy number variation1nstd229human GRCh38 chr5: 176,274,501-176,277,000 , GRCh37.p13 chr5: 175,701,504-175,704,003 SIMC1
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