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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978056insertion1nstd209human GRCh38 chr11: 82,728,870-82,728,870 , GRCh37.p13 chr11: 82,439,912-82,439,912 FAM181B
    nsv5923122copy number variation1nstd209human GRCh38 chr11: 82,696,400-82,750,465 , GRCh37.p13 chr11: 82,407,442-82,461,507 FAM181B
    nsv5848279copy number variation2nstd209human GRCh38 chr11: 82,732,359-82,733,831 , GRCh37.p13 chr11: 82,443,401-82,444,873 FAM181B
    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
    nsv4840094copy number variation1nstd200human GRCh37 chr11: 82,434,773-82,441,878 , GRCh38.p12 chr11: 82,723,731-82,730,836 FAM181B
    nsv4608954copy number variation1nstd183human GRCh37 chr11: 82,265,877-82,441,837 , GRCh38.p12 chr11: 82,554,835-82,730,795 RPS28P7, FAM181B
    nsv4603035copy number variation1nstd183human GRCh37 chr11: 82,264,444-82,440,868 , GRCh38.p12 chr11: 82,553,402-82,729,826 FAM181B, RPS28P7
    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
    nsv3921008copy number variation1nstd102humanPathogenic NCBI36 chr11: 77,750,902-85,554,070 , GRCh38 chr11: 78,362,208-86,165,380 , GRCh37 chr11: 78,073,254-85,876,422 CCDC83, ZNF75CP, 70 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
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3904761copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,053,454-113,316,236 , GRCh38.p12 chr11: 80,342,410-113,445,514 RPS6P16, CTSC, 449 more genes
    nsv3901209copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,771,852-90,851,187 , GRCh38.p12 chr11: 82,060,810-91,118,019 RPL7AP54, TRIM77, 124 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
    nsv3897292copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,318,996-96,116,221 , GRCh38.p12 chr11: 80,607,952-96,383,057 FAM181B, LOC107984371, 218 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
    nsv2732449copy number variation1nstd130human NCBI36 chr11: 73,243,988-90,057,911 , GRCh37.p13 chr11: 73,566,340-90,418,263 , GRCh38.p12 chr11: 73,855,295-90,685,095 , FOLH1B, 271 more genes
    nsv1601545short tandem repeat1nstd128human GRCh37 chr11: 82,444,854-82,444,873 , GRCh38.p12 chr11: 82,733,812-82,733,831 FAM181B
    nsv1598957short tandem repeat9nstd128human GRCh37 chr11: 82,439,914-82,439,925 , GRCh38.p12 chr11: 82,728,872-82,728,883 FAM181B
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