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Items: 1 to 20 of 102

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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
    nsv7073567inversion1nstd229human GRCh38 chr11: 73,812,649-75,298,624 , GRCh37.p13 chr11: 73,523,694-75,009,668 LIPT2, RNF169, 51 more genes
    nsv6906674copy number variation1nstd229human GRCh38 chr11: 74,417,177-74,565,327 , GRCh37.p13 chr11: 74,128,222-74,276,372 LIPT2-AS1, LOC107984356, 3 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
    nsv6132277copy number variation1nstd213human GRCh37 chr11: 74,020,000-74,240,001 , GRCh38.p12 chr11: 74,308,955-74,528,956 PGM2L1, HNRNPA1P40, 9 more genes
    nsv5494028copy number variation1nstd206human GRCh38 chr11: 74,225,600-74,828,943 , GRCh37.p13 chr11: 73,936,645-74,539,988 RNF169, MIR4696, 19 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
    nsv4612428copy number variation1nstd183human GRCh37 chr11: 74,195,370-74,220,688 , GRCh38.p12 chr11: 74,484,325-74,509,643 LIPT2, LOC107984356, 1 more genes
    nsv4555128insertion1nstd166human GRCh37.p13 chr11: 74,203,685-74,203,685 , GRCh38.p12 chr11: 74,492,640-74,492,640 LIPT2-AS1, LIPT2
    nsv4418797copy number variation1nstd174human GRCh37 chr11: 73,936,645-74,539,988 , GRCh38.p12 chr11: 74,225,600-74,828,943 POLD3, CHRDL2, 19 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
    esv3864544copy number variation1estd219human GRCh37 chr11: 74,027,538-74,539,358 , GRCh38.p12 chr11: 74,316,493-74,828,313 CYCSP27, LIPT2, 17 more genes
    esv3864539copy number variation6estd219human GRCh37 chr11: 73,936,495-74,540,138 , GRCh38.p12 chr11: 74,225,450-74,829,093 POLD3, PPME1, 19 more genes
    nsv2732449copy number variation1nstd130human NCBI36 chr11: 73,243,988-90,057,911 , GRCh37.p13 chr11: 73,566,340-90,418,263 , GRCh38.p12 chr11: 73,855,295-90,685,095 , FOLH1B, 271 more genes
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