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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
    nsv4702623copy number variation1nstd195human GRCh37 chr11: 72,214,651-72,354,851 , GRCh38.p12 chr11: 72,503,607-72,643,807 ART2P, PDE2A, 7 more genes
    nsv3967408insertion1nstd168human GRCh37.p13 chr11: 72,279,200-72,346,436 , GRCh38 chr11: 72,568,156-72,635,392 PDE2A, MIR139, 4 more genes
    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
    nsv3235283insertion9nstd152human GRCh38 chr11: 72,568,156-72,615,784 , GRCh37.p13 chr11: 72,279,200-72,326,828 PDE2A, MIR139, 3 more genes
    nsv3142081copy number variation1nstd151human GRCh37 chr11: 71,668,270-74,638,536 , GRCh38.p12 chr11: 71,957,224-74,927,491 , RPL36AP38, 92 more genes
    nsv1595996short tandem repeat1nstd128human GRCh37 chr11: 72,282,974-72,282,985 , GRCh38.p12 chr11: 72,571,930-72,571,941 LINC01537
    nsv1595995short tandem repeat1nstd128human GRCh37 chr11: 72,280,874-72,280,896 , GRCh38.p12 chr11: 72,569,830-72,569,852 LINC01537
    nsv1592608short tandem repeat2nstd128human GRCh37 chr11: 72,284,648-72,284,681 , GRCh38.p12 chr11: 72,573,604-72,573,637 LINC01537
    nsv1360814copy number variation1nstd122human NCBI36 chr11: 71,957,198-72,140,282 , GRCh37.p13 chr11: 72,279,550-72,462,634 , GRCh38.p12 chr11: 72,568,506-72,751,589 PDE2A, PDE2A-AS2, 8 more genes
    nsv1132999inversion1nstd106human GRCh37 chr11: 1,620,508-89,079,908 , GRCh38.p12 chr11: 1,599,278-89,346,740 , ACTN3, 2007 more genes
    nsv1125301inversion1nstd106human GRCh37 chr11: 48,489,096-88,979,496 , GRCh38.p12 chr11: 48,467,544-89,246,328 , MRPL49, 1130 more genes
    esv3807849tandem duplication1estd192human GRCh37 chr11: 16,492,879-90,295,791 , GRCh38.p12 chr11: 16,471,332-90,562,623 , LOC107984356, 1605 more genes
    esv3801718tandem duplication2estd192human GRCh37 chr11: 64,845,409-117,019,859 , GRCh38.p12 chr11: 65,077,937-117,149,143 , MMP12, 992 more genes
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