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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5501616copy number variation1nstd206human GRCh38 chr11: 95,832,657-95,833,957 , GRCh37.p13 chr11: 95,565,821-95,567,121 MTMR2, CEP57
    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
    nsv5348151translocation1nstd200human GRCh38 chr11: 95,833,957-95,833,957 , GRCh38 chr11: 95,832,657-95,832,657 , GRCh37.p13 chr11: 95,567,121-95,567,121 , GRCh37.p13 chr11: 95,565,821-95,565,821 MTMR2, CEP57
    nsv5318663copy number variation1nstd204human GRCh37.p13 chr11: 95,565,799-95,567,141 , GRCh38.p13 chr11: 95,832,635-95,833,977 CEP57, MTMR2
    nsv5278851copy number variation1nstd204human GRCh38.p13 chr11: 95,832,650-95,833,999 , GRCh37.p13 chr11: 95,565,814-95,567,163 CEP57, MTMR2
    nsv5131920mobile element insertion1nstd203human GRCh38 chr11: 95,804,946-95,804,960 , GRCh37.p13 chr11: 95,538,110-95,538,124 CEP57
    nsv5127522mobile element insertion1nstd203human GRCh38 chr11: 95,806,166-95,806,179 , GRCh37.p13 chr11: 95,539,330-95,539,343 CEP57
    nsv5037979inversion1nstd200human GRCh38 chr11: 93,899,952-96,855,215 , GRCh37.p13 chr11: 93,633,118-96,726,215 , GPR83, 52 more genes
    nsv4989185copy number variation1nstd200human GRCh38 chr11: 95,804,688-95,804,852 , GRCh37.p13 chr11: 95,537,852-95,538,016 CEP57
    nsv4845043copy number variation1nstd200human GRCh37 chr11: 95,537,852-95,538,016 , GRCh38.p12 chr11: 95,804,688-95,804,852 CEP57
    nsv4844418copy number variation1nstd200human GRCh37 chr11: 95,565,821-95,567,121 , GRCh38.p12 chr11: 95,832,657-95,833,957 CEP57, MTMR2
    nsv4600369copy number variation1nstd183human GRCh37 chr11: 95,520,985-95,527,885 , GRCh38.p12 chr11: 95,787,821-95,794,721 CEP57, FAM76B
    nsv4421926copy number variation1nstd174human GRCh37 chr11: 95,565,792-95,567,130 , GRCh38.p12 chr11: 95,832,628-95,833,966 CEP57, MTMR2
    nsv4203526copy number variation1nstd166human GRCh37.p13 chr11: 95,519,850-95,525,500 , GRCh38.p12 chr11: 95,786,686-95,792,336 FAM76B, CEP57
    nsv4192663copy number variation1nstd166human GRCh37.p13 chr11: 95,565,821-95,567,121 , GRCh38.p12 chr11: 95,832,657-95,833,957 MTMR2, CEP57
    nsv3922508copy number variation1nstd102humanPathogenic GRCh38 chr11: 85,242,847-102,920,097 , GRCh37 chr11: 84,953,891-102,738,968 , NCBI36 chr11: 84,631,539-102,296,037 AMOTL1, LNCRNA-IUR, 240 more genes
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3916760copy number variation1nstd102humanUncertain significance NCBI36 chr11: 93,697,096-95,454,478 , GRCh38 chr11: 94,324,282-96,081,666 , GRCh37 chr11: 94,057,448-95,814,830 SESN3, SRSF8BP, 36 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 PLS1P1, SNORA25, 349 more genes
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