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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094183copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,146,421-75,283,128 , GRCh38.p12 chr11: 71,435,375-75,572,083 LOC112268078, LRTOMT, 142 more genes
    nsv7076680inversion1nstd229human GRCh38 chr11: 72,466,691-73,774,399 , GRCh37.p13 chr11: 72,177,735-73,485,444 OR8R1P, PDE2A, 33 more genes
    nsv7075390inversion1nstd229human GRCh38 chr11: 72,466,687-73,774,399 , GRCh37.p13 chr11: 72,177,731-73,485,444 RAB6A, MIR139, 33 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6314007copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,567,724-72,488,649 , GRCh38.p12 chr11: 71,856,678-72,777,604 STARD10, PDE2A, 38 more genes
    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
    nsv4455833copy number variation1nstd102humanUncertain significance GRCh37 chr11: 72,291,927-72,349,390 , GRCh38.p12 chr11: 72,580,883-72,638,346 PDE2A, LOC105369377, 3 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
    nsv3155389copy number variation1nstd151human GRCh37 chr11: 72,308,551-72,408,536 , GRCh38.p12 chr11: 72,597,507-72,697,491 PDE2A, ARAP1, 4 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
    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
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