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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
    nsv5355353translocation1nstd200human GRCh38 chr11: 72,139,219-72,139,219 , GRCh38 chr11: 72,177,195-72,177,195 , GRCh37.p13 chr11: 71,850,263-71,850,263 , GRCh37.p13 chr11: 71,888,239-71,888,239 FOLR3, FOLR3P1
    nsv5331481translocation1nstd200human GRCh37 chr11: 71,850,263-71,850,263 , GRCh37 chr11: 71,888,239-71,888,239 , GRCh38.p12 chr11: 72,139,219-72,139,219 , GRCh38.p12 chr11: 72,177,195-72,177,195 FOLR3, FOLR3P1
    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
    nsv4985128copy number variation1nstd200human GRCh38 chr11: 72,135,955-72,172,560 , GRCh37.p13 chr11: 71,847,001-71,883,604 FOLR1P1, FOLR3P1, 1 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
    nsv4425434copy number variation1nstd174human GRCh37 chr11: 71,847,797-71,890,984 , GRCh38.p12 chr11: 72,136,751-72,179,940 FOLR1P1, FOLR3, 1 more genes
    nsv4415121copy number variation1nstd174human GRCh37 chr11: 71,846,443-71,892,793 , GRCh38.p12 chr11: 72,135,397-72,181,749 FOLR3, FOLR1P1, 1 more genes
    nsv4376986copy number variation1nstd173human GRCh37 chr11: 71,847,808-71,873,232 , GRCh38.p12 chr11: 72,136,762-72,162,188 FOLR1P1, FOLR3
    nsv4372237copy number variation2nstd173human GRCh37 chr11: 71,847,228-71,873,232 , GRCh38.p12 chr11: 72,136,182-72,162,188 FOLR3, FOLR1P1
    nsv4205732copy number variation1nstd166human GRCh37.p13 chr11: 71,848,500-71,886,000 , GRCh38.p12 chr11: 72,137,454-72,174,956 FOLR3P1, FOLR3, 1 more genes
    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
    nsv3155081copy number variation1nstd151human GRCh37 chr11: 71,846,997-71,847,169 , GRCh38.p12 chr11: 72,135,951-72,136,123 FOLR3
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