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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4984480copy number variation1nstd200human GRCh38 chr11: 47,563,410-47,608,721 , GRCh37.p13 chr11: 47,584,962-47,630,273 CELF1, KBTBD4, 6 more genes
    nsv4848564copy number variation1nstd200human GRCh37 chr11: 47,606,392-47,607,205 , GRCh38.p12 chr11: 47,584,840-47,585,653 , GRCh38.p12 chr11|NW_019805496.1: 12,666-13,479 NDUFS3, FAM180B
    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
    nsv3924778copy number variation1nstd102humanPathogenic GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131 F2, PSMC3, 140 more genes
    nsv3917203copy number variation1nstd102humanBenign NCBI36 chr11: 47,546,389-47,573,697 , GRCh37 chr11: 47,589,813-47,617,121 , GRCh38 chr11: 47,568,261-47,595,569 NDUFS3, FAM180B, 4 more genes
    nsv3915177copy number variation1nstd102humanUncertain significance NCBI36 chr11: 47,562,712-47,746,515 , GRCh37.p13 chr11: 47,606,136-47,789,939 , GRCh38.p12 chr11: 47,584,584-47,768,387 , GRCh38.p12 chr11|NW_019805496.1: 12,410-200,754 NDUFS3, C1QTNF4, 4 more genes
    nsv3914709copy number variation1nstd102humanPathogenic GRCh38 chr11: 46,840,454-48,643,003 , GRCh37 chr11: 46,862,005-48,664,555 , NCBI36 chr11: 46,818,581-48,621,131 CELF1, C1QTNF4, 56 more genes
    nsv3914563copy number variation1nstd102humanLikely pathogenic NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735 ACP2, ARHGAP1, 143 more genes
    nsv3913842copy number variation1nstd102humanPathogenic GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735 MIR3160-1, RPS20P26, 162 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
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3168776inversion1nstd158human GRCh37 chr11: 37,074,771-61,357,521 , GRCh38.p12 chr11: 37,053,221-61,590,049 , ACP2, 535 more genes
    nsv3168425copy number variation1nstd158human GRCh37 chr11: 3,543,079-67,662,509 , GRCh38.p12 chr11: 3,521,849-67,895,038 , ACP2, 1535 more genes
    nsv3143339copy number variation1nstd151human GRCh37 chr11: 47,602,074-47,606,038 , GRCh38.p12 chr11: 47,580,522-47,584,486 , GRCh38.p12 chr11|NW_019805496.1: 8,348-12,312 NDUFS3
    nsv1583257short tandem repeat6nstd128human GRCh37 chr11: 47,606,232-47,606,248 , GRCh38.p12 chr11: 47,584,680-47,584,696 , GRCh38.p12 chr11|NW_019805496.1: 12,506-12,522 NDUFS3, FAM180B
    nsv1583256short tandem repeat2nstd128human GRCh37 chr11: 47,602,712-47,602,725 , GRCh38.p12 chr11: 47,581,160-47,581,173 , GRCh38.p12 chr11|NW_019805496.1: 8,986-8,999 NDUFS3
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