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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094072copy number variation1nstd102humanUncertain significance GRCh37 chr13: 31,033,232-33,638,323 , GRCh38.p12 chr13: 30,459,095-33,064,186 N4BP2L2, RNY1P4, 37 more genes
    nsv7093387copy number variation1nstd102humannot provided GRCh37 chr13: 31,841,196-36,667,007 , GRCh38.p12 chr13: 31,267,059-36,092,870 VDAC1P12, LOC107984589, 44 more genes
    nsv7093180copy number variation1nstd102humanUncertain significance GRCh37 chr13: 33,590,493-33,590,597 , GRCh38 chr13: 33,016,355-33,016,459 KL
    nsv7093066copy number variation1nstd102humanUncertain significance GRCh37 chr13: 33,590,495-33,590,602 , GRCh38 chr13: 33,016,357-33,016,464 KL
    nsv7075032inversion1nstd229human GRCh38 chr13: 30,791,896-33,130,541 , GRCh37.p13 chr13: 31,366,033-33,704,678 BRCA2, TEX26, 31 more genes
    nsv7069550inversion1nstd229human GRCh38 chr13: 31,196,586-33,130,540 , GRCh37.p13 chr13: 31,770,723-33,704,677 BRCA2, ZAR1L, 21 more genes
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6957099copy number variation1nstd229human GRCh38 chr13: 33,055,374-33,056,331 , GRCh37.p13 chr13: 33,629,511-33,630,468 KL
    nsv6950623copy number variation1nstd229human GRCh38 chr13: 33,028,401-33,035,800 , GRCh37.p13 chr13: 33,602,539-33,609,937 KL
    nsv6945103copy number variation1nstd229human GRCh38 chr13: 33,036,360-33,036,410 , GRCh37.p13 chr13: 33,610,497-33,610,547 KL
    nsv6943446copy number variation1nstd229human GRCh38 chr13: 33,035,067-33,037,225 , GRCh37.p13 chr13: 33,609,204-33,611,362 KL
    nsv6942114copy number variation1nstd229human GRCh38 chr13: 33,040,720-33,046,110 , GRCh37.p13 chr13: 33,614,857-33,620,247 KL
    nsv6924346copy number variation1nstd229human GRCh38 chr13: 31,409,618-33,230,882 , GRCh37.p13 chr13: 31,983,755-33,805,019 TOMM22P3, IFIT1P1, 19 more genes
    nsv6637377copy number variation1nstd102humanUncertain significance GRCh37 chr13: 33,504,270-34,507,428 , GRCh38.p12 chr13: 32,930,132-33,933,291 TOMM22P3, RFC3, 7 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
    nsv6622042copy number variation1nstd224human GRCh37 chr13: 33,376,118-34,281,440 , GRCh38.p12 chr13: 32,801,980-33,707,303 KL, STARD13, 6 more genes
    nsv6589214inversion1nstd223human GRCh38 chr13: 33,051,298-33,052,255 , GRCh37.p13 chr13: 33,625,435-33,626,392 KL
    nsv6487406copy number variation1nstd223human GRCh38 chr13: 33,053,023-33,053,478 , GRCh37.p13 chr13: 33,627,160-33,627,615 KL
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 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
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