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Items: 1 to 20 of 459

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7057034inversion1nstd229human GRCh38 chr4: 184,049,673-184,581,802 , GRCh37.p13 chr4: 184,970,826-185,502,956 MYL12BP2, LINC02363, 11 more genes
    nsv7054725inversion1nstd229human GRCh38 chr4: 178,850,585-188,333,056 , GRCh37.p13 chr4: 179,771,739-189,254,210 RPL6P16, LOC105377568, 125 more genes
    nsv7054658inversion1nstd229human GRCh38 chr4: 183,954,061-185,864,650 , GRCh37.p13 chr4: 184,875,214-186,785,804 IRF2, LOC105377590, 39 more genes
    nsv7053482inversion1nstd229human GRCh38 chr4: 184,332,325-184,386,056 , GRCh37.p13 chr4: 185,253,478-185,307,210 IRF2, LINC02363, 1 more genes
    nsv7053039inversion1nstd229human GRCh38 chr4: 183,766,927-184,811,271 , GRCh37.p13 chr4: 184,688,080-185,732,425 LOC105377582, ENPP6, 18 more genes
    nsv7049252inversion1nstd229human GRCh38 chr4: 184,328,564-184,385,842 , GRCh37.p13 chr4: 185,249,717-185,306,996 IRF2, LINC02363, 1 more genes
    nsv7048281inversion1nstd229human GRCh38 chr4: 177,590,230-186,282,308 , GRCh37.p13 chr4: 178,511,384-187,203,462 STOX2, LINC01098, 105 more genes
    nsv7042799inversion1nstd229human GRCh38 chr4: 183,807,135-184,532,873 , GRCh37.p13 chr4: 184,728,288-185,454,027 LOC100421006, RN7SL28P, 11 more genes
    nsv6757405copy number variation1nstd229human GRCh38 chr4: 184,393,588-184,393,975 , GRCh37.p13 chr4: 185,314,742-185,315,129 IRF2
    nsv6756944copy number variation1nstd229human GRCh38 chr4: 184,402,149-185,513,891 , GRCh37.p13 chr4: 185,323,303-186,435,045 LINC02365, SNX25, 27 more genes
    nsv6756370copy number variation1nstd229human GRCh38 chr4: 184,467,030-184,471,777 , GRCh37.p13 chr4: 185,388,184-185,392,931 IRF2
    nsv6755274copy number variation1nstd229human GRCh38 chr4: 184,426,174-184,426,535 , GRCh37.p13 chr4: 185,347,328-185,347,689 IRF2
    nsv6755160copy number variation1nstd229human GRCh38 chr4: 184,430,293-184,430,338 , GRCh37.p13 chr4: 185,351,447-185,351,492 IRF2
    nsv6754539copy number variation1nstd229human GRCh38 chr4: 184,421,313-184,423,025 , GRCh37.p13 chr4: 185,342,467-185,344,179 IRF2
    nsv6754164copy number variation1nstd229human GRCh38 chr4: 184,460,509-184,466,130 , GRCh37.p13 chr4: 185,381,663-185,387,284 IRF2
    nsv6753101copy number variation1nstd229human GRCh38 chr4: 184,413,688-184,413,845 , GRCh37.p13 chr4: 185,334,842-185,334,999 IRF2
    nsv6751914copy number variation1nstd229human GRCh38 chr4: 184,382,513-184,383,035 , GRCh37.p13 chr4: 185,303,667-185,304,189 IRF2, LINC02362
    nsv6751002copy number variation1nstd229human GRCh38 chr4: 184,467,918-184,470,740 , GRCh37.p13 chr4: 185,389,072-185,391,894 IRF2
    nsv6749813copy number variation1nstd229human GRCh38 chr4: 184,387,414-184,387,592 , GRCh37.p13 chr4: 185,308,568-185,308,746 IRF2
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