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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975979insertion1nstd209human GRCh38 chr11: 118,581,933-118,581,933 , GRCh37.p13 chr11: 118,452,648-118,452,648 , GRCh37.p13 chr11|NW_003871072.2: 207,371-207,371 ARCN1
    nsv5917018copy number variation1nstd209human GRCh38 chr11: 118,598,167-118,598,220 , GRCh37.p13 chr11: 118,468,882-118,468,935 , GRCh37.p13 chr11|NW_003871072.2: 223,605-223,658 ARCN1
    nsv5336914translocation1nstd200human GRCh37 chr11: 118,468,915-118,468,915 , GRCh37 chr3: 176,990,345-176,990,345 , GRCh38.p12 chr11: 118,598,200-118,598,200 , GRCh38.p12 chr3: 177,272,557-177,272,557 ARCN1
    nsv5126194mobile element insertion1nstd203human GRCh38 chr11: 118,575,752-118,575,766 , GRCh37.p13 chr11|NW_003871072.2: 201,190-201,204 , GRCh37.p13 chr11: 118,446,467-118,446,481 ARCN1, IFT46
    nsv5123194mobile element insertion1nstd203human GRCh38 chr11: 118,598,040-118,598,052 , GRCh37.p13 chr11|NW_003871072.2: 223,478-223,490 , GRCh37.p13 chr11: 118,468,755-118,468,767 ARCN1
    nsv4989350copy number variation1nstd200human GRCh38 chr11: 118,562,787-118,577,917 , GRCh37.p13 chr11: 118,433,502-118,448,632 , GRCh37.p13 chr11|NW_003871072.2: 188,225-203,355 ARCN1, IFT46
    nsv4980930copy number variation1nstd200human GRCh38 chr11: 118,581,838-118,581,896 , GRCh37.p13 chr11: 118,452,553-118,452,611 , GRCh37.p13 chr11|NW_003871072.2: 207,276-207,334 ARCN1
    nsv4829470copy number variation1nstd200human GRCh37 chr11: 118,433,502-118,448,632 , GRCh38.p12 chr11: 118,562,787-118,577,917 IFT46, ARCN1
    nsv4756863insertion1nstd199human GRCh37 chr11: 118,452,619-118,452,619 , GRCh38.p12 chr11: 118,581,904-118,581,904 ARCN1
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4683551copy number variation9nstd102humanUncertain significance, Pathogenic GRCh37 chr11: 117,856,768-118,972,385 , GRCh38.p12 chr11: 117,986,053-119,101,675 MIR6716, TREHP1, 48 more genes
    nsv4675236copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,280,670-119,650,105 , GRCh38.p12 chr11: 118,409,955-119,779,396 SETP16, UPK2, 59 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4614078copy number variation1nstd183human GRCh37 chr11: 118,435,866-118,448,544 , GRCh38.p12 chr11: 118,565,151-118,577,829 ARCN1, IFT46
    nsv4604292copy number variation1nstd183human GRCh37 chr11: 118,444,303-118,448,544 , GRCh38.p12 chr11: 118,573,588-118,577,829 IFT46, ARCN1
    nsv4527997copy number variation1nstd166human GRCh37.p13 chr11: 118,463,046-118,463,111 , GRCh38.p12 chr11: 118,592,331-118,592,396 RNU6-1157P, ARCN1
    nsv4515750mobile element insertion1nstd166human GRCh37.p13 chr11: 118,458,691-118,458,691 , GRCh38.p12 chr11: 118,587,976-118,587,976 ARCN1
    nsv4455281copy number variation1nstd102humanPathogenic GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576 NTM-AS1, LOC403312, 369 more genes
    nsv4451218copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,007,722-119,170,511 , GRCh38.p12 chr11: 118,137,007-119,299,801 ABCG4, CCDC153, 52 more genes
    nsv4377454copy number variation1nstd173human GRCh37 chr11: 118,355,769-118,621,008 , GRCh38.p12 chr11: 118,485,054-118,750,298 PHLDB1, IFT46, 13 more genes
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