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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
    nsv7061071inversion1nstd229human GRCh38 chr11: 64,416,765-64,622,794 , GRCh37.p13 chr11: 64,184,237-64,390,266 NRXN2, SLC22A11, 3 more genes
    nsv6916883copy number variation1nstd229human GRCh38 chr11: 64,562,914-64,569,432 , GRCh37.p13 chr11: 64,330,386-64,336,904 SLC22A11
    nsv6906376copy number variation1nstd229human GRCh38 chr11: 64,571,503-64,571,735 , GRCh37.p13 chr11: 64,338,975-64,339,207 SLC22A11
    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
    nsv6904685copy number variation1nstd229human GRCh38 chr11: 64,565,153-64,568,892 , GRCh37.p13 chr11: 64,332,625-64,336,364 SLC22A11
    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
    nsv6460001copy number variation1nstd223human GRCh38 chr11: 64,547,262-64,558,066 , GRCh37.p13 chr11: 64,314,734-64,325,538 SLC22A11
    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
    nsv6132184copy number variation1nstd213human GRCh37 chr11: 64,210,000-64,390,001 , GRCh38.p12 chr11: 64,442,528-64,622,529 NRXN2, SLC22A11, 2 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv4985041copy number variation1nstd200human GRCh38 chr11: 64,547,239-64,558,088 , GRCh37.p13 chr11: 64,314,711-64,325,560 SLC22A11
    nsv4979798copy number variation1nstd200human GRCh38 chr11: 64,562,913-64,569,427 , GRCh37.p13 chr11: 64,330,385-64,336,899 SLC22A11
    nsv4844077copy number variation1nstd200human GRCh37 chr11: 64,314,683-64,325,556 , GRCh38.p12 chr11: 64,547,211-64,558,084 SLC22A11
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4679239copy number variation1nstd189human GRCh37.p13 chr11: 64,222,931-65,140,850 , GRCh38.p12 chr11: 64,455,459-65,373,379 ARL2, VPS51, 52 more genes
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