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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911453copy number variation1nstd209human GRCh38 chr11: 72,109,926-72,110,084 , GRCh37.p13 chr11: 71,820,972-71,821,130 ANAPC15, LRTOMT
    nsv5496223copy number variation1nstd206human GRCh38 chr11: 72,110,227-72,110,493 , GRCh37.p13 chr11: 71,821,273-71,821,539 ANAPC15, LRTOMT
    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
    nsv5278677copy number variation1nstd204human GRCh37.p13 chr11: 71,772,747-71,889,344 , GRCh38.p13 chr11: 72,061,701-72,178,300 FOLR3, NUMA1, 7 more genes
    nsv4987247copy number variation1nstd200human GRCh38 chr11: 72,105,324-72,106,404 , GRCh37.p13 chr11: 71,816,370-71,817,450 LRTOMT, ANAPC15
    nsv4829495copy number variation1nstd200human GRCh37 chr11: 71,816,370-71,817,448 , GRCh38.p12 chr11: 72,105,324-72,106,402 LRTOMT, ANAPC15
    nsv4715783copy number variation1nstd195human GRCh37 chr11: 71,663,751-71,844,051 , GRCh38.p12 chr11: 71,952,705-72,133,005 NUMA1, IL18BP, 7 more genes
    nsv4681893copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,401-71,907,241 , GRCh38.p12 chr11: 71,435,355-72,196,197 OR7E128P, ZNF705EP, 39 more genes
    nsv4202421copy number variation1nstd166human GRCh37.p13 chr11: 71,801,000-71,829,000 , GRCh38.p12 chr11: 72,089,954-72,117,954 LAMTOR1, LRTOMT, 1 more genes
    nsv4199357copy number variation1nstd166human GRCh37.p13 chr11: 71,812,000-71,826,000 , GRCh38.p12 chr11: 72,100,954-72,114,954 LRTOMT, ANAPC15, 1 more genes
    nsv3956580copy number variation1nstd168human GRCh38 chr11: 72,111,055-72,122,455 , GRCh37.p13 chr11: 71,822,101-71,833,501 ANAPC15, LRTOMT
    nsv3921153copy number variation1nstd102humanUncertain significance GRCh38 chr11: 71,164,008-72,309,374 , GRCh37 chr11: 71,088,949-72,020,418 , NCBI36 chr11: 70,552,702-71,698,066 LOC220077, PHOX2A, 47 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
    nsv3142081copy number variation1nstd151human GRCh37 chr11: 71,668,270-74,638,536 , GRCh38.p12 chr11: 71,957,224-74,927,491 , RPL36AP38, 92 more genes
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