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Items: 1 to 20 of 82

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058775inversion1nstd229human GRCh38 chr11: 78,228,684-78,557,765 , GRCh37.p13 chr11: 77,939,730-78,268,811 ZNF75CP, LOC101928896, 5 more genes
    nsv6916305copy number variation1nstd229human GRCh38 chr11: 78,428,760-78,432,545 , GRCh37.p13 chr11: 78,139,806-78,143,591 LINC02728
    nsv6458936copy number variation1nstd223human GRCh38 chr11: 78,424,252-78,424,584 , GRCh37.p13 chr11: 78,135,298-78,135,630 LINC02728
    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
    nsv6313961copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,855,209-98,002,445 , GRCh38.p12 chr11: 78,144,163-98,131,717 MTND5P38, XIAPP2, 252 more genes
    nsv6132279copy number variation1nstd213human GRCh37 chr11: 78,140,000-78,310,001 , GRCh38.p12 chr11: 78,428,954-78,598,956 NARS2, LINC02728, 4 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
    nsv5277499copy number variation1nstd204human GRCh38.p13 chr11: 78,418,101-78,426,100 , GRCh37.p13 chr11: 78,129,147-78,137,146 LINC02728, GAB2
    nsv4206957copy number variation1nstd166human GRCh37.p13 chr11: 78,139,797-78,143,588 , GRCh38.p12 chr11: 78,428,751-78,432,542 LINC02728
    nsv3921121copy number variation1nstd102humanPathogenic GRCh38 chr11: 75,941,754-98,357,960 , NCBI36 chr11: 75,330,446-97,733,898 , GRCh37 chr11: 75,652,798-98,228,688 LOC105369441, RNU6-1135P, 296 more genes
    nsv3921008copy number variation1nstd102humanPathogenic NCBI36 chr11: 77,750,902-85,554,070 , GRCh38 chr11: 78,362,208-86,165,380 , GRCh37 chr11: 78,073,254-85,876,422 CCDC83, ZNF75CP, 70 more genes
    nsv3913977copy number variation1nstd102humanPathogenic GRCh37 chr11: 77,943,882-106,650,146 , GRCh38 chr11: 78,232,836-106,779,420 , NCBI36 chr11: 77,621,530-106,155,356 PLS1P1, SNORA25, 349 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
    nsv3155022copy number variation1nstd151human GRCh37 chr11: 76,924,903-78,443,625 , GRCh38.p12 chr11: 77,213,858-78,732,580 USP35, LOC107984369, 33 more genes
    esv4010893copy number variation1estd233human GRCh37 chr11: 77,872,000-78,330,000 , GRCh38.p12 chr11: 78,160,954-78,618,955 GAB2, USP35, 10 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
    nsv1598494short tandem repeat4nstd128human GRCh37 chr11: 78,134,166-78,134,181 , GRCh38.p12 chr11: 78,423,120-78,423,135 LINC02728
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