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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093772copy number variation1nstd102humanPathogenic GRCh37 chr11: 61,197,619-61,552,680 , GRCh38.p12 chr11: 61,430,147-61,785,208 LOC105369331, CPSF7, 12 more genes
    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
    nsv7076174inversion1nstd229human GRCh38 chr11: 57,437,573-64,138,990 , GRCh37.p13 chr11: 57,205,046-63,906,462 RNU2-2P, SLC43A1, 299 more genes
    nsv6917433copy number variation1nstd229human GRCh38 chr11: 61,472,401-62,010,600 , GRCh37.p13 chr11: 61,239,873-61,778,072 LOC105369329, FADS3, 24 more genes
    nsv6916971copy number variation1nstd229human GRCh38 chr11: 61,477,022-61,488,177 , GRCh37.p13 chr11: 61,244,494-61,255,649 SAXO4
    nsv6915036copy number variation1nstd229human GRCh38 chr11: 61,477,104-61,488,176 , GRCh37.p13 chr11: 61,244,576-61,255,648 SAXO4
    nsv6911999copy number variation1nstd229human GRCh38 chr11: 61,477,097-61,488,181 , GRCh37.p13 chr11: 61,244,569-61,255,653 SAXO4
    nsv6909200copy number variation1nstd229human GRCh38 chr11: 61,458,001-62,069,400 , GRCh37.p13 chr11: 61,225,473-61,836,872 RPS2P37, BEST1, 25 more genes
    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
    nsv6904042copy number variation1nstd229human GRCh38 chr11: 61,456,701-62,012,000 , GRCh37.p13 chr11: 61,224,173-61,779,472 LOC399900, LRRC10B, 24 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
    nsv6463098copy number variation1nstd223human GRCh38 chr11: 61,477,106-61,488,301 , GRCh37.p13 chr11: 61,244,578-61,255,773 SAXO4
    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
    nsv6315474copy number variation1nstd102humanPathogenic GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199 TRR-TCT3-2, OR4A41P, 494 more genes
    nsv5915570copy number variation1nstd209human GRCh38 chr11: 61,477,122-61,488,222 , GRCh37.p13 chr11: 61,244,594-61,255,694 SAXO4
    nsv5852932copy number variation1nstd209human GRCh38 chr11: 61,482,102-61,483,293 , GRCh37.p13 chr11: 61,249,574-61,250,765 SAXO4
    nsv5851459copy number variation1nstd209human GRCh38 chr11: 61,477,056-61,488,090 , GRCh37.p13 chr11: 61,244,528-61,255,562 SAXO4
    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
    nsv5325627inversion1nstd204human GRCh37.p13 chr11: 58,669,453-61,321,541 , GRCh38.p13 chr11: 58,901,980-61,554,069 , CD5, 118 more genes
    nsv4885672inversion1nstd200human GRCh37 chr11: 58,669,461-61,321,541 , GRCh38.p12 chr11: 58,901,988-61,554,069 , MS4A2, 118 more genes
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