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Items: 1 to 20 of 209

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv7064476inversion1nstd229human GRCh38 chr11: 123,462,060-125,907,500 , GRCh37.p13 chr11: 123,332,768-125,777,395 STT3A, OR8G1, 101 more genes
    nsv6917999copy number variation1nstd229human GRCh38 chr11: 124,667,401-124,676,600 , GRCh37.p13 chr11: 124,537,297-124,546,496 SIAE, SPA17
    nsv6917949copy number variation1nstd229human GRCh38 chr11: 124,685,679-124,690,123 , GRCh37.p13 chr11: 124,555,575-124,560,019 SPA17
    nsv6916629copy number variation1nstd229human GRCh38 chr11: 124,677,241-124,788,089 , GRCh37.p13 chr11: 124,547,137-124,657,985 ESAM, VSIG2, 5 more genes
    nsv6916077copy number variation1nstd229human GRCh38 chr11: 124,575,701-124,974,400 , GRCh37.p13 chr11: 124,445,597-124,844,296 SIAE, HEPACAM, 19 more genes
    nsv6911168copy number variation1nstd229human GRCh38 chr11: 124,676,528-124,680,866 , GRCh37.p13 chr11: 124,546,424-124,550,762 SIAE, SPA17
    nsv6907989copy number variation1nstd229human GRCh38 chr11: 124,676,804-124,677,587 , GRCh37.p13 chr11: 124,546,700-124,547,483 SPA17
    nsv6907856copy number variation1nstd229human GRCh38 chr11: 124,539,858-124,705,388 , GRCh37.p13 chr11: 124,409,754-124,575,284 OR8Q1P, TBRG1, 6 more genes
    nsv6902792copy number variation1nstd229human GRCh38 chr11: 124,678,128-124,678,189 , GRCh37.p13 chr11: 124,548,024-124,548,085 SPA17
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6475341copy number variation1nstd223human GRCh38 chr11: 124,682,504-124,692,565 , GRCh37.p13 chr11: 124,552,400-124,562,461 SPA17
    nsv6463888copy number variation1nstd223human GRCh38 chr11: 124,539,858-124,705,383 , GRCh37.p13 chr11: 124,409,754-124,575,279 SPA17, SIAE, 6 more genes
    nsv6459873copy number variation1nstd223human GRCh38 chr11: 124,682,517-124,686,839 , GRCh37.p13 chr11: 124,552,413-124,556,735 SPA17
    nsv6457517copy number variation1nstd223human GRCh38 chr11: 124,696,845-124,697,316 , GRCh37.p13 chr11: 124,566,741-124,567,212 SPA17
    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
    nsv6309101copy number variation1nstd102humanUncertain significance GRCh37 chr11: 124,506,847-124,543,604 , GRCh38.p12 chr11: 124,636,951-124,673,708 SIAE, SPA17, 1 more genes
    nsv6309036copy number variation3nstd102humanUncertain significance GRCh37 chr11: 123,504,851-126,163,012 , GRCh38.p12 chr11: 123,634,143-126,293,117 CDON, PKNOX2-DT, 113 more genes
    nsv6291285copy number variation1nstd102humanUncertain significance GRCh37 chr11: 124,296,335-124,560,100 , GRCh38.p12 chr11: 124,426,439-124,690,204 OR8B8, SPA17, 12 more genes
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