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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6917817copy number variation1nstd229human GRCh38 chr11: 75,778,301-75,843,500 , GRCh37.p13 chr11: 75,489,346-75,554,545 DGAT2, UVRAG-DT, 1 more genes
    nsv6460796copy number variation1nstd223human GRCh38 chr11: 75,778,334-75,843,552 , GRCh37.p13 chr11: 75,489,379-75,554,597 DGAT2, UVRAG-DT, 1 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
    nsv6132278copy number variation1nstd213human GRCh37 chr11: 75,150,000-75,550,001 , GRCh38.p12 chr11: 75,438,955-75,838,956 MAP6, DGAT2, 11 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
    nsv4987356copy number variation1nstd200human GRCh38 chr11: 75,814,412-75,814,591 , GRCh37.p13 chr11: 75,525,457-75,525,636 UVRAG, UVRAG-DT
    nsv3962113copy number variation1nstd168human GRCh38 chr11: 75,792,984-75,816,930 , GRCh37.p13 chr11: 75,504,029-75,527,975 DGAT2, UVRAG-DT, 1 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
    nsv3228442copy number variation1nstd152human GRCh38 chr11: 75,815,219-75,816,930 , GRCh37.p13 chr11: 75,526,264-75,527,975 UVRAG-DT, UVRAG
    nsv3153513copy number variation1nstd151human GRCh37 chr11: 75,298,101-75,623,088 , GRCh38.p12 chr11: 75,587,056-75,912,044 , LOC105369391, 10 more genes
    nsv3142968copy number variation1nstd151human GRCh37 chr11: 74,676,806-76,893,648 , GRCh38.p12 chr11: 74,965,761-77,182,603 , LOC107984358, 56 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
    nsv1596492short tandem repeat2nstd128human GRCh37 chr11: 75,526,279-75,526,316 , GRCh38.p12 chr11: 75,815,234-75,815,271 UVRAG-DT, UVRAG
    nsv1596491short tandem repeat7nstd128human GRCh37 chr11: 75,524,911-75,524,928 , GRCh38.p12 chr11: 75,813,866-75,813,883 UVRAG-DT, UVRAG
    nsv1594553short tandem repeat1nstd128human GRCh37 chr11: 75,525,009-75,525,020 , GRCh38.p12 chr11: 75,813,964-75,813,975 UVRAG, UVRAG-DT
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