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Items: 1 to 20 of 344

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143936insertion1nstd232human GRCh37.p13 chr11: 62,153,911-62,153,911 , GRCh38.p12 chr11: 62,386,439-62,386,439 ASRGL1
    nsv7094091copy number variation1nstd102humanUncertain significance GRCh37 chr11: 62,156,585-62,159,756 , GRCh38.p12 chr11: 62,389,113-62,392,284 ASRGL1
    nsv7093694copy number variation2nstd102humanUncertain significance GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878 VPS37C, POLR2G, 298 more genes
    nsv7077001inversion1nstd229human GRCh38 chr11: 61,961,332-62,482,821 , GRCh37.p13 chr11: 61,728,804-62,250,293 SCGB2A1, INCENP, 16 more genes
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv7073441inversion1nstd229human GRCh38 chr11: 62,381,836-62,385,119 , GRCh37.p13 chr11: 62,149,308-62,152,591 ASRGL1
    nsv7059171inversion1nstd229human GRCh38 chr11: 62,343,209-62,344,176 , GRCh37.p13 chr11: 62,110,681-62,111,648 ASRGL1
    nsv6917296copy number variation1nstd229human GRCh38 chr11: 62,340,370-62,340,558 , GRCh37.p13 chr11: 62,107,842-62,108,030 ASRGL1
    nsv6916040copy number variation1nstd229human GRCh38 chr11: 62,371,990-62,374,709 , GRCh37.p13 chr11: 62,139,462-62,142,181 RCC2P6, ASRGL1
    nsv6915598copy number variation1nstd229human GRCh38 chr11: 62,398,783-62,401,128 , GRCh37.p13 chr11: 62,166,255-62,168,600 ASRGL1
    nsv6914105copy number variation1nstd229human GRCh38 chr11: 62,347,423-62,355,098 , GRCh37.p13 chr11: 62,114,895-62,122,570 ASRGL1
    nsv6913764copy number variation1nstd229human GRCh38 chr11: 62,325,417-62,389,620 , GRCh37.p13 chr11: 62,092,889-62,157,092 ASRGL1, NPM1P35, 1 more genes
    nsv6911557copy number variation1nstd229human GRCh38 chr11: 62,320,220-62,405,620 , GRCh37.p13 chr11: 62,087,692-62,173,092 RCC2P6, NPM1P35, 1 more genes
    nsv6911130copy number variation1nstd229human GRCh38 chr11: 62,366,701-62,385,400 , GRCh37.p13 chr11: 62,134,173-62,152,872 RCC2P6, ASRGL1
    nsv6910261copy number variation1nstd229human GRCh38 chr11: 62,363,535-62,369,754 , GRCh37.p13 chr11: 62,131,007-62,137,226 ASRGL1
    nsv6910053copy number variation1nstd229human GRCh38 chr11: 62,363,901-63,050,100 , GRCh37.p13 chr11: 62,131,373-62,817,572 MIR6747, TMEM179B, 54 more genes
    nsv6908094copy number variation1nstd229human GRCh38 chr11: 62,358,134-62,365,616 , GRCh37.p13 chr11: 62,125,606-62,133,088 ASRGL1
    nsv6906079copy number variation1nstd229human GRCh38 chr11: 62,367,001-62,385,100 , GRCh37.p13 chr11: 62,134,473-62,152,572 ASRGL1, RCC2P6
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6904633copy number variation1nstd229human GRCh38 chr11: 62,370,232-62,370,385 , GRCh37.p13 chr11: 62,137,704-62,137,857 ASRGL1, RCC2P6
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