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Items: 1 to 20 of 754

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148115copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,775,348-51,221,365 , GRCh38.p12 chr15: 49,483,151-50,929,168 RNA5SP395, AHCYP7, 24 more genes
    nsv7146834copy number variation1nstd232human GRCh37.p13 chr15: 49,842,085-49,842,134 , GRCh38.p12 chr15: 49,549,888-49,549,937 FAM227B, LOC105370811
    nsv7140302insertion1nstd232human GRCh37.p13 chr15: 49,664,440-49,664,440 , GRCh38.p12 chr15: 49,372,243-49,372,243 FAM227B
    nsv7076699inversion1nstd229human GRCh38 chr15: 49,344,882-49,349,730 , GRCh37.p13 chr15: 49,637,079-49,641,927 GALK2, FAM227B
    nsv7076356inversion1nstd229human GRCh38 chr15: 49,451,408-49,451,515 , GRCh37.p13 chr15: 49,743,605-49,743,712 FAM227B, FGF7
    nsv7067773inversion1nstd229human GRCh38 chr15: 49,468,891-49,474,630 , GRCh37.p13 chr15: 49,761,088-49,766,827 FGF7, FAM227B
    nsv7067502inversion1nstd229human GRCh38 chr15: 48,513,881-51,354,383 , GRCh37.p13 chr15: 48,806,078-51,646,580 NDUFAF4P1, MIR4713, 49 more genes
    nsv7067143inversion1nstd229human GRCh38 chr15: 49,376,802-49,376,819 , GRCh37.p13 chr15: 49,668,999-49,669,016 FAM227B
    nsv7066363inversion1nstd229human GRCh38 chr15: 49,373,173-49,406,150 , GRCh37.p13 chr15: 49,665,370-49,698,347 FAM227B
    nsv6977745copy number variation1nstd229human GRCh38 chr15: 49,548,295-49,558,636 , GRCh37.p13 chr15: 49,840,492-49,850,833 LOC105370811, FAM227B
    nsv6977389copy number variation1nstd229human GRCh38 chr15: 49,380,629-49,381,585 , GRCh37.p13 chr15: 49,672,826-49,673,782 FAM227B
    nsv6976204copy number variation1nstd229human GRCh38 chr15: 49,519,196-49,525,698 , GRCh37.p13 chr15: 49,811,393-49,817,895 LOC105370811, FAM227B
    nsv6976048copy number variation1nstd229human GRCh38 chr15: 49,511,901-49,538,800 , GRCh37.p13 chr15: 49,804,098-49,830,997 FAM227B, LOC105370811
    nsv6975949copy number variation1nstd229human GRCh38 chr15: 49,615,933-49,622,879 , GRCh37.p13 chr15: 49,908,130-49,915,076 DTWD1, FAM227B
    nsv6975528copy number variation1nstd229human GRCh38 chr15: 49,383,201-49,392,100 , GRCh37.p13 chr15: 49,675,398-49,684,297 FAM227B
    nsv6975419copy number variation1nstd229human GRCh38 chr15: 49,330,542-49,333,858 , GRCh37.p13 chr15: 49,622,739-49,626,055 FAM227B, GALK2
    nsv6975274copy number variation1nstd229human GRCh38 chr15: 49,471,514-49,571,398 , GRCh37.p13 chr15: 49,763,711-49,863,595 FGF7, FAM227B, 1 more genes
    nsv6975109copy number variation1nstd229human GRCh38 chr15: 49,609,493-49,609,855 , GRCh37.p13 chr15: 49,901,690-49,902,052 FAM227B
    nsv6975091copy number variation1nstd229human GRCh38 chr15: 49,557,332-49,572,173 , GRCh37.p13 chr15: 49,849,529-49,864,370 FAM227B, LOC105370811
    nsv6975085copy number variation1nstd229human GRCh38 chr15: 49,359,601-49,363,700 , GRCh37.p13 chr15: 49,651,798-49,655,897 GALK2, LOC100420615, 1 more genes
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