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Items: 1 to 20 of 185

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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
    nsv7072709inversion1nstd229human GRCh38 chr13: 43,918,456-43,982,271 , GRCh37.p13 chr13: 44,492,592-44,556,407 DGKZP1, LOC105370182
    nsv7064333inversion1nstd229human GRCh38 chr13: 43,956,373-44,045,555 , GRCh37.p13 chr13: 44,530,509-44,619,691 NRAD1, DGKZP1, 1 more genes
    nsv6952643copy number variation1nstd229human GRCh38 chr13: 43,996,890-44,001,092 , GRCh37.p13 chr13: 44,571,026-44,575,228 LOC105370182
    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
    nsv6946207copy number variation1nstd229human GRCh38 chr13: 44,001,801-44,051,300 , GRCh37.p13 chr13: 44,575,937-44,625,436 LOC105370182, NRAD1
    nsv6939301copy number variation1nstd229human GRCh38 chr13: 44,001,323-44,001,403 , GRCh37.p13 chr13: 44,575,459-44,575,539 LOC105370182
    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
    nsv6622170copy number variation1nstd224human GRCh37 chr13: 44,551,293-44,607,279 , GRCh38.p12 chr13: 43,977,157-44,033,143 LOC105370182, NRAD1
    nsv6485690copy number variation1nstd223human GRCh38 chr13: 44,011,995-44,012,389 , GRCh37.p13 chr13: 44,586,131-44,586,525 LOC105370182
    nsv6479279copy number variation1nstd223human GRCh38 chr13: 43,995,318-43,995,751 , GRCh37.p13 chr13: 44,569,454-44,569,887 LOC105370182
    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
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