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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062534inversion1nstd229human GRCh38 chr11: 83,132,580-86,771,462 , GRCh37.p13 chr11: 82,843,622-86,482,504 CCDC83, LOC100421303, 44 more genes
    nsv6915527copy number variation1nstd229human GRCh38 chr11: 82,974,601-83,470,600 , GRCh37.p13 chr11: 82,685,643-83,181,643 CYCSP28, DLG2, 14 more genes
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6637282copy number variation1nstd102humanUncertain significance GRCh37 chr11: 82,859,094-83,324,406 , GRCh38.p12 chr11: 83,148,052-83,613,363 CKS1BP4, ANKRD42, 9 more genes
    nsv6593710inversion1nstd223human GRCh38 chr11: 83,172,676-83,173,423 , GRCh37.p13 chr11: 82,883,718-82,884,465 PCF11
    nsv6592392inversion1nstd223human GRCh38 chr11: 83,179,292-83,179,910 , GRCh37.p13 chr11: 82,890,334-82,890,952 PCF11
    nsv6585044inversion1nstd223human GRCh38 chr11: 83,175,297-83,175,685 , GRCh37.p13 chr11: 82,886,339-82,886,727 PCF11
    nsv6576738inversion1nstd223human GRCh38 chr11: 83,175,146-83,175,572 , GRCh37.p13 chr11: 82,886,188-82,886,614 PCF11
    nsv6461041copy number variation1nstd223human GRCh38 chr11: 83,172,616-83,174,106 , GRCh37.p13 chr11: 82,883,658-82,885,148 PCF11
    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
    nsv6248251mobile element insertion1nstd215human GRCh38 chr11: 83,160,361-83,160,361 , GRCh37.p13 chr11: 82,871,403-82,871,403 PCF11
    nsv6132285copy number variation1nstd213human GRCh37 chr11: 82,730,000-83,280,001 , GRCh38.p12 chr11: 83,018,958-83,568,958 DLG2, PCF11, 15 more genes
    nsv6089443insertion1nstd212human GRCh38 chr11: 83,183,870-83,183,870 , GRCh37.p13 chr11: 82,894,912-82,894,912 PCF11, ANKRD42-DT, 1 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
    nsv5184693mobile element insertion1nstd203human GRCh38 chr11: 83,155,955-83,155,955 , GRCh37.p13 chr11: 82,866,997-82,866,997 PCF11
    nsv5131168mobile element insertion1nstd203human GRCh38 chr11: 83,170,864-83,170,877 , GRCh37.p13 chr11: 82,881,906-82,881,919 PCF11
    nsv5130672mobile element insertion1nstd203human GRCh38 chr11: 83,170,867-83,170,877 , GRCh37.p13 chr11: 82,881,909-82,881,919 PCF11
    nsv4989096copy number variation1nstd200human GRCh38 chr11: 83,172,616-83,174,108 , GRCh37.p13 chr11: 82,883,658-82,885,150 PCF11
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