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Items: 1 to 20 of 144

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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
    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
    nsv6950560copy number variation1nstd229human GRCh38 chr13: 44,574,469-44,574,497 , GRCh37.p13 chr13: 45,148,605-45,148,633 TSC22D1, TSC22D1-AS1
    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
    nsv6594306inversion1nstd223human GRCh38 chr13: 44,580,572-44,581,104 , GRCh37.p13 chr13: 45,154,708-45,155,240 TSC22D1-AS1
    nsv6487599copy number variation1nstd223human GRCh38 chr13: 44,573,101-44,576,400 , GRCh37.p13 chr13: 45,147,237-45,150,536 TSC22D1-AS1, TSC22D1
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314198copy number variation1nstd102humanPathogenic GRCh37 chr13: 44,573,371-53,324,137 , GRCh38.p12 chr13: 43,999,235-52,750,002 PCNPP5, NRAD1, 189 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
    nsv6132648copy number variation1nstd213human GRCh37 chr13: 45,080,000-45,160,001 , GRCh38.p12 chr13: 44,505,864-44,585,865 TSC22D1, TSC22D1-AS1
    nsv6132644copy number variation1nstd213human GRCh37 chr13: 38,830,000-56,580,001 , GRCh38.p12 chr13: 38,255,863-56,005,867 , ATP7B, 305 more genes
    nsv6132557copy number variation1nstd213human GRCh37 chr13: 44,840,000-52,410,001 , GRCh38.p12 chr13: 44,265,864-51,835,865 , RCBTB2, 160 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
    nsv5713947mobile element insertion1nstd211human GRCh38 chr13: 44,579,871-44,579,871 , GRCh37.p13 chr13: 45,154,007-45,154,007 TSC22D1-AS1
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