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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5912279copy number variation1nstd209human GRCh38 chr11: 116,779,086-116,779,231 , GRCh37.p13 chr11: 116,649,802-116,649,947 ZPR1
    nsv5502729copy number variation1nstd206human GRCh38 chr11: 116,773,051-116,773,109 , GRCh37.p13 chr11: 116,643,767-116,643,825 BUD13, ZPR1
    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
    nsv5348330translocation1nstd200human GRCh38 chr11: 116,772,665-116,772,665 , GRCh38 chr11: 116,772,749-116,772,749 , GRCh37.p13 chr11: 116,643,381-116,643,381 , GRCh37.p13 chr11: 116,643,465-116,643,465 ZPR1, BUD13
    nsv5197174mobile element insertion1nstd203human GRCh38 chr11: 116,776,823-116,776,840 , GRCh37.p13 chr11: 116,647,539-116,647,556 ZPR1
    nsv5035338inversion1nstd200human GRCh38 chr11: 114,039,980-117,481,226 , GRCh37.p13 chr11: 113,910,702-117,351,941 , LINC02703, 56 more genes
    nsv4745189copy number variation1nstd199human GRCh37 chr11: 116,650,813-116,650,955 , GRCh38.p12 chr11: 116,780,097-116,780,239 ZPR1
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 LINC02732, LINC02698, 198 more genes
    nsv4203656copy number variation1nstd166human GRCh37.p13 chr11: 116,649,805-116,649,948 , GRCh38.p12 chr11: 116,779,089-116,779,232 ZPR1
    nsv4200855copy number variation1nstd166human GRCh37.p13 chr11: 116,643,767-116,643,825 , GRCh38.p12 chr11: 116,773,051-116,773,109 ZPR1, BUD13
    nsv3966345copy number variation1nstd168human GRCh38 chr11: 116,758,203-116,826,769 , GRCh37.p13 chr11: 116,628,919-116,697,485 ZPR1, BUD13, 2 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3914316copy number variation1nstd102humanPathogenic NCBI36 chr11: 115,812,352-117,422,156 , GRCh38 chr11: 116,436,425-118,046,231 , GRCh37 chr11: 116,307,142-117,916,946 LOC653303, BUD13, 31 more genes
    nsv3913230copy number variation1nstd102humanPathogenic GRCh38 chr11: 113,444,446-120,648,921 , NCBI36 chr11: 112,820,378-120,024,840 , GRCh37 chr11: 113,315,168-120,519,630 ARHGEF12, LOC105369526, 169 more genes
    nsv3912905copy number variation1nstd102humanPathogenic GRCh38 chr11: 112,864,326-131,189,315 , GRCh37 chr11: 112,832,130-131,059,210 , NCBI36 chr11: 112,240,259-130,564,420 SLC37A2, OR6X1, 416 more genes
    nsv3911601copy number variation1nstd102humanUncertain significance NCBI36 chr11: 115,023,598-116,957,808 , GRCh37 chr11: 115,518,388-117,452,598 , GRCh38 chr11: 115,647,670-117,581,883 ZPR1, LOC653303, 32 more genes
    nsv3909122copy number variation1nstd102humanPathogenic GRCh37 chr11: 115,215,434-120,559,928 , GRCh38.p12 chr11: 115,344,715-120,689,219 LOC107984393, CENATAC-DT, 136 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
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