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Items: 1 to 20 of 314

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7069463inversion1nstd229human GRCh38 chr11: 64,441,902-64,755,854 , GRCh37.p13 chr11: 64,209,374-64,523,326 NRXN2, SLC22A12, 5 more genes
    nsv7065702inversion1nstd229human GRCh38 chr11: 64,606,791-64,606,878 , GRCh37.p13 chr11: 64,374,263-64,374,350 NRXN2
    nsv7061071inversion1nstd229human GRCh38 chr11: 64,416,765-64,622,794 , GRCh37.p13 chr11: 64,184,237-64,390,266 NRXN2, SLC22A11, 3 more genes
    nsv6916400copy number variation1nstd229human GRCh38 chr11: 64,674,403-64,688,771 , GRCh37.p13 chr11: 64,441,875-64,456,243 NRXN2
    nsv6914596copy number variation1nstd229human GRCh38 chr11: 64,712,001-64,712,062 , GRCh37.p13 chr11: 64,479,473-64,479,534 NRXN2
    nsv6911699copy number variation1nstd229human GRCh38 chr11: 64,625,749-64,625,813 , GRCh37.p13 chr11: 64,393,221-64,393,285 NRXN2
    nsv6909721copy number variation1nstd229human GRCh38 chr11: 64,707,301-64,710,400 , GRCh37.p13 chr11: 64,474,773-64,477,872 NRXN2
    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
    nsv6903911copy number variation1nstd229human GRCh38 chr11: 64,622,701-64,755,900 , GRCh37.p13 chr11: 64,390,173-64,523,372 PYGM, NRXN2-AS1, 2 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6902839copy number variation1nstd229human GRCh38 chr11: 64,698,345-64,698,525 , GRCh37.p13 chr11: 64,465,817-64,465,997 NRXN2
    nsv6901220copy number variation1nstd229human GRCh38 chr11: 64,658,588-64,659,504 , GRCh37.p13 chr11: 64,426,060-64,426,976 NRXN2
    nsv6900782copy number variation1nstd229human GRCh38 chr11: 64,687,001-64,691,200 , GRCh37.p13 chr11: 64,454,473-64,458,672 NRXN2
    nsv6898537copy number variation1nstd229human GRCh38 chr11: 64,680,139-64,683,117 , GRCh37.p13 chr11: 64,447,611-64,450,589 NRXN2
    nsv6590888inversion1nstd223human GRCh38 chr11: 64,664,327-64,666,501 , GRCh37.p13 chr11: 64,431,799-64,433,973 NRXN2
    nsv6466380copy number variation1nstd223human GRCh38 chr11: 64,707,277-64,710,428 , GRCh37.p13 chr11: 64,474,749-64,477,900 NRXN2
    nsv6465715copy number variation1nstd223human GRCh38 chr11: 64,662,001-64,664,200 , GRCh37.p13 chr11: 64,429,473-64,431,672 NRXN2
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6248140mobile element insertion1nstd215human GRCh38 chr11: 64,707,586-64,707,586 , GRCh37.p13 chr11: 64,475,058-64,475,058 NRXN2
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