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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5647454insertion1nstd207human GRCh38 chr11: 72,828,926-72,828,926 , GRCh37.p13 chr11: 72,539,971-72,539,971 ATG16L2
    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
    nsv4713821copy number variation1nstd195human GRCh37 chr11: 72,354,901-72,655,251 , GRCh38.p12 chr11: 72,643,857-72,944,206 , ARAP1-AS2, 11 more genes
    nsv4574900mobile element insertion1nstd166human GRCh37.p13 chr11: 72,527,324-72,527,324 , GRCh38.p12 chr11: 72,816,279-72,816,279 ATG16L2
    nsv4568733sequence alteration1nstd166human GRCh37.p13 chr11: 72,535,892-72,536,472 , GRCh38.p12 chr11: 72,824,847-72,825,427 ATG16L2
    nsv4493384mobile element insertion1nstd166human GRCh37.p13 chr11: 72,531,313-72,531,313 , GRCh38.p12 chr11: 72,820,268-72,820,268 ATG16L2
    nsv3919985copy number variation1nstd102humanPathogenic NCBI36 chr11: 70,668,528-72,528,680 , GRCh37.p13 chr11: 70,990,880-72,851,032 , GRCh38.p12 chr11: 71,279,834-73,139,987 OR7E128P, OR7E87P, 68 more genes
    nsv3916301copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216 RN7SL786P, LIPT2-AS1, 146 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 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
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3157267copy number variation1nstd151human GRCh37 chr11: 72,539,771-72,552,631 , GRCh38.p12 chr11: 72,828,726-72,841,586 ATG16L2, FCHSD2
    nsv3154501copy number variation1nstd151human GRCh37 chr11: 72,537,215-72,538,343 , GRCh38.p12 chr11: 72,826,170-72,827,298 ATG16L2
    nsv3152880copy number variation1nstd151human GRCh37 chr11: 72,539,771-72,600,993 , GRCh38.p12 chr11: 72,828,726-72,889,948 RNU6-672P, ATG16L2, 1 more genes
    nsv3150833copy number variation1nstd151human GRCh37 chr11: 72,399,497-72,534,011 , GRCh38.p12 chr11: 72,688,452-72,822,966 , MIR4692, 6 more genes
    nsv3149112copy number variation2nstd151human GRCh37 chr11: 72,528,798-72,537,873 , GRCh38.p12 chr11: 72,817,753-72,826,828 ATG16L2
    nsv3148857copy number variation1nstd151human GRCh37 chr11: 72,539,925-72,695,264 , GRCh38.p12 chr11: 72,828,880-72,984,219 RPL15P16, RNU6-672P, 2 more genes
    nsv3147778copy number variation1nstd151human GRCh37 chr11: 72,423,238-72,528,924 , GRCh38.p12 chr11: 72,712,193-72,817,879 , STARD10, 4 more genes
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