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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926661copy number variation1nstd209human GRCh38 chr11: 82,906,652-82,907,122 , GRCh37.p13 chr11: 82,617,694-82,618,164 DDIAS
    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
    nsv5361508translocation1nstd200human GRCh38 chr11: 82,907,123-82,907,123 , GRCh38 chr11: 82,906,652-82,906,652 , GRCh37.p13 chr11: 82,617,694-82,617,694 , GRCh37.p13 chr11: 82,618,165-82,618,165 DDIAS
    nsv5131698mobile element insertion1nstd203human GRCh38 chr11: 82,918,756-82,918,769 , GRCh37.p13 chr11: 82,629,798-82,629,811 DDIAS
    nsv4989093copy number variation1nstd200human GRCh38 chr11: 82,906,789-83,029,404 , GRCh37.p13 chr11: 82,617,831-82,740,446 RAB30, RPL7AP54, 1 more genes
    nsv4989092copy number variation1nstd200human GRCh38 chr11: 82,893,559-82,913,386 , GRCh37.p13 chr11: 82,604,601-82,624,428 PRCP, DDIAS
    nsv4843532copy number variation1nstd200human GRCh37 chr11: 82,604,601-82,624,428 , GRCh38.p12 chr11: 82,893,559-82,913,386 DDIAS, PRCP
    nsv4729116copy number variation1nstd102humanUncertain significance GRCh37 chr11: 82,618,269-83,454,773 , GRCh38.p12 chr11: 82,907,227-83,743,730 RAB30, RAB30-DT, 18 more genes
    nsv4197761copy number variation1nstd166human GRCh37.p13 chr11: 82,638,501-82,638,585 , GRCh38.p12 chr11: 82,927,459-82,927,543 DDIAS
    nsv3923065copy number variation1nstd102humanUncertain significance NCBI36 chr11: 82,262,002-82,391,597 , GRCh37.p13 chr11: 82,584,354-82,713,949 , GRCh38.p12 chr11: 82,873,312-83,002,907 DDIAS, PRCP, 2 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
    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
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