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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7065663inversion1nstd229human GRCh38 chr13: 43,893,709-43,893,733 , GRCh37.p13 chr13: 44,467,845-44,467,869 LACC1
    nsv6953986copy number variation1nstd229human GRCh38 chr13: 43,657,457-43,920,826 , GRCh37.p13 chr13: 44,231,593-44,494,962 ENOX1, LACC1, 1 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
    nsv6939435copy number variation1nstd229human GRCh38 chr13: 43,512,071-43,930,110 , GRCh37.p13 chr13: 44,086,207-44,504,246 ENOX1, CCDC122, 1 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6484710copy number variation1nstd223human GRCh38 chr13: 43,512,028-43,930,110 , GRCh37.p13 chr13: 44,086,164-44,504,246 CCDC122, LACC1, 1 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6291480copy number variation1nstd102humanUncertain significance GRCh37 chr13: 43,688,967-45,630,698 , GRCh38.p12 chr13: 43,114,831-45,056,563 LINC00400, ENOX1-AS2, 31 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6248982mobile element insertion1nstd215human GRCh38 chr13: 43,887,914-43,887,914 , GRCh37.p13 chr13: 44,462,050-44,462,050 LACC1
    nsv6132647copy number variation1nstd213human GRCh37 chr13: 44,100,000-44,540,001 , GRCh38.p12 chr13: 43,525,864-43,965,865 ENOX1, LACC1, 1 more genes
    nsv6132644copy number variation1nstd213human GRCh37 chr13: 38,830,000-56,580,001 , GRCh38.p12 chr13: 38,255,863-56,005,867 , ATP7B, 305 more genes
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6132484copy number variation1nstd213human GRCh37 chr13: 38,830,000-44,630,001 , GRCh38.p12 chr13: 38,255,863-44,055,865 CALM2P3, ELF1, 99 more genes
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