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Items: 1 to 20 of 939

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148188copy number variation1nstd102humanPathogenic GRCh38 chr5: 88,189,536-93,784,597 , GRCh37.p13 chr5: 87,485,353-93,120,303 RPS3AP22, LOC105379078, 49 more genes
    nsv7056868inversion1nstd229human GRCh38 chr5: 93,725,287-93,730,964 , GRCh37.p13 chr5: 93,060,993-93,066,670 ARB2A
    nsv7053325inversion1nstd229human GRCh38 chr5: 94,111,155-94,125,622 , GRCh37.p13 chr5: 93,446,860-93,461,327 LOC105379087, ARB2A
    nsv7049143inversion1nstd229human GRCh38 chr5: 93,730,864-93,735,586 , GRCh37.p13 chr5: 93,066,570-93,071,292 ARB2A, POU5F2
    nsv7044198inversion1nstd229human GRCh38 chr5: 93,856,097-99,790,151 , GRCh37.p13 chr5: 93,191,803-99,125,855 FAM81B, LOC107986365, 78 more genes
    nsv7040673inversion1nstd229human GRCh38 chr5: 93,633,598-93,641,490 , GRCh37.p13 chr5: 92,969,304-92,977,196 ARB2A
    nsv7039765inversion1nstd229human GRCh38 chr5: 94,085,197-94,087,699 , GRCh37.p13 chr5: 93,420,902-93,423,404 ARB2A
    nsv6778039copy number variation1nstd229human GRCh38 chr5: 94,058,378-94,067,728 , GRCh37.p13 chr5: 93,394,083-93,403,433 ARB2A
    nsv6777946copy number variation1nstd229human GRCh38 chr5: 93,864,580-93,864,615 , GRCh37.p13 chr5: 93,200,286-93,200,321 ARB2A
    nsv6777760copy number variation1nstd229human GRCh38 chr5: 93,974,041-93,974,159 , GRCh37.p13 chr5: 93,309,746-93,309,864 ARB2A
    nsv6776730copy number variation1nstd229human GRCh38 chr5: 94,085,714-94,098,304 , GRCh37.p13 chr5: 93,421,419-93,434,009 ARB2A
    nsv6776379copy number variation1nstd229human GRCh38 chr5: 93,943,734-93,949,634 , GRCh37.p13 chr5: 93,279,439-93,285,339 ARB2A
    nsv6776003copy number variation1nstd229human GRCh38 chr5: 93,947,036-93,947,079 , GRCh37.p13 chr5: 93,282,741-93,282,784 ARB2A
    nsv6774642copy number variation1nstd229human GRCh38 chr5: 93,979,669-94,007,025 , GRCh37.p13 chr5: 93,315,374-93,342,730 ARB2A
    nsv6773959copy number variation1nstd229human GRCh38 chr5: 93,791,998-93,797,449 , GRCh37.p13 chr5: 93,127,704-93,133,155 ARB2A
    nsv6772669copy number variation1nstd229human GRCh38 chr5: 93,766,202-93,771,456 , GRCh37.p13 chr5: 93,101,908-93,107,162 ARB2A
    nsv6772076copy number variation1nstd229human GRCh38 chr5: 93,765,701-93,771,100 , GRCh37.p13 chr5: 93,101,407-93,106,806 ARB2A
    nsv6771668copy number variation1nstd229human GRCh38 chr5: 93,894,007-93,894,214 , GRCh37.p13 chr5: 93,229,713-93,229,920 ARB2A
    nsv6771094copy number variation1nstd229human GRCh38 chr5: 93,903,704-93,945,446 , GRCh37.p13 chr5: 93,239,410-93,281,151 ARB2A
    nsv6771036copy number variation1nstd229human GRCh38 chr5: 93,838,940-93,856,126 , GRCh37.p13 chr5: 93,174,646-93,191,832 ARB2A
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