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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076887inversion1nstd229human GRCh38 chr13: 42,736,299-43,232,604 , GRCh37.p13 chr13: 43,310,435-43,806,740 DNAJC15, FAM216B, 10 more genes
    nsv7075189inversion1nstd229human GRCh38 chr13: 38,938,572-45,892,931 , GRCh37.p13 chr13: 39,512,709-46,467,066 TPT1-AS1, AKAP11, 136 more genes
    nsv7075009inversion1nstd229human GRCh38 chr13: 42,255,185-44,636,659 , GRCh37.p13 chr13: 42,829,321-45,210,795 SERP2, DNAJC15, 35 more genes
    nsv7073451inversion1nstd229human GRCh38 chr13: 39,843,646-49,674,098 , GRCh37.p13 chr13: 40,417,783-50,248,234 CYCSP34, FNDC3A, 195 more genes
    nsv7060789inversion1nstd229human GRCh38 chr13: 38,967,784-43,058,064 , GRCh37.p13 chr13: 39,541,921-43,632,200 RGCC, RAC1P3, 79 more genes
    nsv7058535inversion1nstd229human GRCh38 chr13: 42,774,872-43,134,427 , GRCh37.p13 chr13: 43,349,008-43,708,563 LOC105370178, LINC00428, 8 more genes
    nsv6957461copy number variation1nstd229human GRCh38 chr13: 42,155,232-43,166,161 , GRCh37.p13 chr13: 42,729,368-43,740,297 TNFSF11, LINC00400, 15 more genes
    nsv6952483copy number variation1nstd229human GRCh38 chr13: 41,848,658-47,157,739 , GRCh37.p13 chr13: 42,422,794-47,731,874 TSC22D1-AS1, LINC00330, 105 more genes
    nsv6948072copy number variation1nstd229human GRCh38 chr13: 42,780,820-42,910,779 , GRCh37.p13 chr13: 43,354,956-43,484,915 FAM216B, EPSTI1, 3 more genes
    nsv6947672copy number variation1nstd229human GRCh38 chr13: 42,787,387-43,302,865 , GRCh37.p13 chr13: 43,361,523-43,877,001 EPSTI1, LINC00400, 10 more genes
    nsv6947209copy number variation1nstd229human GRCh38 chr13: 42,736,567-43,346,765 , GRCh37.p13 chr13: 43,310,703-43,920,901 LOC105370179, EPSTI1, 10 more genes
    nsv6946838copy number variation1nstd229human GRCh38 chr13: 42,788,976-43,304,064 , GRCh37.p13 chr13: 43,363,112-43,878,200 LINC00400, LINC00428, 10 more genes
    nsv6946654copy number variation1nstd229human GRCh38 chr13: 42,781,468-43,257,909 , GRCh37.p13 chr13: 43,355,604-43,832,045 EPSTI1, ENOX1, 10 more genes
    nsv6946279copy number variation1nstd229human GRCh38 chr13: 42,770,395-43,341,880 , GRCh37.p13 chr13: 43,344,531-43,916,016 ZDHHC4P1, ENOX1, 10 more genes
    nsv6946143copy number variation1nstd229human GRCh38 chr13: 42,588,265-43,144,864 , GRCh37.p13 chr13: 43,162,401-43,719,000 EPSTI1, LINC00400, 9 more genes
    nsv6942769copy number variation1nstd229human GRCh38 chr13: 42,767,645-42,899,274 , GRCh37.p13 chr13: 43,341,781-43,473,410 LOC107984611, LINC00428, 3 more genes
    nsv6941433copy number variation1nstd229human GRCh38 chr13: 42,766,420-42,839,987 , GRCh37.p13 chr13: 43,340,556-43,414,123 LINC01050, FAM216B, 1 more genes
    nsv6939012copy number variation1nstd229human GRCh38 chr13: 42,737,446-43,414,387 , GRCh37.p13 chr13: 43,311,582-43,988,523 ZDHHC4P1, ENOX1, 11 more genes
    nsv6637942copy number variation1nstd102humanUncertain significance GRCh37 chr13: 43,354,951-43,411,234 , GRCh38.p12 chr13: 42,780,815-42,837,098 FAM216B, LOC107984611, 1 more genes
    nsv6637284copy number variation1nstd102humanUncertain significance GRCh37 chr13: 43,163,676-43,717,925 , GRCh38.p12 chr13: 42,589,540-43,143,789 LOC105370179, LOC107984611, 9 more genes
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