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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127156insertion1nstd186human GRCh37 chr11: 47,659,912-47,659,912 , GRCh38.p12 chr11: 47,638,360-47,638,360 , GRCh38.p12 chr11|NW_019805496.1: 66,178-66,178 MTCH2
    nsv5923248copy number variation1nstd209human GRCh38 chr11: 47,624,191-47,625,381 , GRCh37.p13 chr11: 47,645,743-47,646,933 MTCH2
    nsv5911747copy number variation1nstd209human GRCh38 chr11: 47,602,077-47,602,380 , GRCh37.p13 chr11: 47,623,629-47,623,932 MTCH2
    nsv5704453mobile element insertion1nstd211human GRCh38 chr11: 47,628,369-47,628,369 , GRCh37.p13 chr11: 47,649,921-47,649,921 MTCH2
    nsv5704135mobile element insertion2nstd211human GRCh38 chr11: 47,640,819-47,640,819 , GRCh37.p13 chr11: 47,662,371-47,662,371 MTCH2
    nsv5661257insertion1nstd207human GRCh38 chr11: 47,638,360-47,638,360 , GRCh37.p13 chr11: 47,659,912-47,659,912 MTCH2
    nsv5550183insertion1nstd206human GRCh38 chr11: 47,638,360-47,638,360 , GRCh37.p13 chr11: 47,659,912-47,659,912 MTCH2
    nsv5513129copy number variation1nstd206human GRCh38 chr11: 47,632,584-47,635,055 , GRCh37.p13 chr11: 47,654,136-47,656,607 MTCH2
    nsv5507520copy number variation1nstd206human GRCh38 chr11: 47,609,372-47,610,667 , GRCh37.p13 chr11: 47,630,924-47,632,219 MTCH2
    nsv5506280copy number variation1nstd206human GRCh38 chr11: 47,608,854-47,610,873 , GRCh37.p13 chr11: 47,630,406-47,632,425 MTCH2
    nsv5494395copy number variation1nstd206human GRCh38 chr11: 47,639,613-47,640,103 , GRCh37.p13 chr11: 47,661,165-47,661,655 MTCH2
    nsv5402916mobile element insertion1nstd206human GRCh38 chr11: 47,628,369-47,628,420 , GRCh37.p13 chr11: 47,649,921-47,649,972 MTCH2
    nsv5396417mobile element insertion1nstd206human GRCh38 chr11: 47,640,819-47,640,855 , GRCh37.p13 chr11: 47,662,371-47,662,407 MTCH2
    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
    nsv5380725copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218 MIR4688, LOC112268075, 58 more genes
    nsv5277406copy number variation1nstd204human GRCh38.p13 chr11: 47,618,901-47,714,500 , GRCh37.p13 chr11: 47,640,453-47,736,052 MTCH2, AGBL2, 1 more genes
    nsv5139995mobile element insertion1nstd203human GRCh38 chr11: 47,638,363-47,638,410 , GRCh37.p13 chr11: 47,659,915-47,659,962 MTCH2
    nsv5139991mobile element insertion1nstd203human GRCh38 chr11: 47,638,380-47,638,410 , GRCh37.p13 chr11: 47,659,932-47,659,962 MTCH2
    nsv5139743mobile element insertion1nstd203human GRCh38 chr11: 47,640,811-47,640,819 , GRCh37.p13 chr11: 47,662,363-47,662,371 MTCH2
    nsv5139570mobile element insertion1nstd203human GRCh38 chr11: 47,638,368-47,638,410 , GRCh37.p13 chr11: 47,659,920-47,659,962 MTCH2
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