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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5510886copy number variation1nstd206human GRCh38 chr11: 114,404,921-114,405,053 , GRCh37.p13 chr11: 114,275,643-114,275,775 RBM7
    nsv5509179copy number variation1nstd206human GRCh38 chr11: 106,441,255-114,742,965 , GRCh37.p13 chr11: 106,311,982-114,613,687 , ATM, 153 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
    nsv5275783copy number variation1nstd204human GRCh38.p13 chr11: 114,401,191-114,405,190 , GRCh37.p13 chr11: 114,271,913-114,275,912 RBM7
    nsv5125966mobile element insertion1nstd203human GRCh38 chr11: 114,398,759-114,398,774 , GRCh37.p13 chr11: 114,269,481-114,269,496 RBM7, C11orf71
    nsv5035338inversion1nstd200human GRCh38 chr11: 114,039,980-117,481,226 , GRCh37.p13 chr11: 113,910,702-117,351,941 , LINC02703, 56 more genes
    nsv4980756copy number variation1nstd200human GRCh38 chr11: 114,402,379-114,402,466 , GRCh37.p13 chr11: 114,273,101-114,273,188 RBM7
    nsv4675680copy number variation1nstd102humanPathogenic GRCh37 chr11: 103,320,065-114,349,787 , GRCh38.p12 chr11: 103,449,337-114,479,065 DRD2, NCAM1, 181 more genes
    nsv4675323copy number variation1nstd102humanPathogenic GRCh37 chr11: 105,699,599-114,524,876 , GRCh38.p12 chr11: 105,828,873-114,654,154 RPSAP50, RNA5SP349, 155 more genes
    nsv4528289copy number variation1nstd166human GRCh37.p13 chr11: 114,177,999-114,420,000 , GRCh38.p12 chr11: 114,307,277-114,549,278 RBM7, NNMT, 8 more genes
    nsv4514151mobile element insertion1nstd166human GRCh37.p13 chr11: 114,270,496-114,270,496 , GRCh38.p12 chr11: 114,399,774-114,399,774 RBM7, C11orf71
    nsv4456659copy number variation1nstd102humanUncertain significance GRCh37 chr11: 110,969,076-114,578,509 , GRCh38.p12 chr11: 111,098,352-114,707,787 RPS29P19, PPP2R1B, 95 more genes
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 LINC02732, LINC02698, 198 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3913230copy number variation1nstd102humanPathogenic GRCh38 chr11: 113,444,446-120,648,921 , NCBI36 chr11: 112,820,378-120,024,840 , GRCh37 chr11: 113,315,168-120,519,630 ARHGEF12, LOC105369526, 169 more genes
    nsv3912905copy number variation1nstd102humanPathogenic GRCh38 chr11: 112,864,326-131,189,315 , GRCh37 chr11: 112,832,130-131,059,210 , NCBI36 chr11: 112,240,259-130,564,420 SLC37A2, OR6X1, 416 more genes
    nsv3910101copy number variation1nstd102humanPathogenic NCBI36 chr11: 87,796,211-113,996,548 , GRCh37.p13 chr11: 88,156,563-114,491,338 , GRCh38.p12 chr11: 88,423,395-114,620,616 PHB1P16, LOC100418884, 385 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
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