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Items: 1 to 20 of 178

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6950072copy number variation1nstd229human GRCh38 chr13: 36,190,480-36,229,043 , GRCh37.p13 chr13: 36,764,617-36,803,180 CCDC169-SOHLH2, SOHLH2, 1 more genes
    nsv6948047copy number variation1nstd229human GRCh38 chr13: 36,177,905-36,215,255 , GRCh37.p13 chr13: 36,752,042-36,789,392 CCDC169-SOHLH2, SOHLH2
    nsv6946173copy number variation1nstd229human GRCh38 chr13: 36,178,821-36,179,063 , GRCh37.p13 chr13: 36,752,958-36,753,200 SOHLH2, CCDC169-SOHLH2
    nsv6945031copy number variation1nstd229human GRCh38 chr13: 36,164,582-36,167,389 , GRCh37.p13 chr13: 36,738,719-36,741,526 SOHLH2, CCDC169-SOHLH2
    nsv6939117copy number variation1nstd229human GRCh38 chr13: 36,176,901-36,187,000 , GRCh37.p13 chr13: 36,751,038-36,761,137 SOHLH2, CCDC169-SOHLH2
    nsv6939053copy number variation1nstd229human GRCh38 chr13: 36,141,901-36,204,500 , GRCh37.p13 chr13: 36,716,038-36,778,637 SOHLH2, CCDC169-SOHLH2, 1 more genes
    nsv6637985copy number variation1nstd102humanUncertain significance GRCh37 chr13: 36,148,057-41,670,428 , GRCh38.p12 chr13: 35,573,920-41,096,292 RPS12P24, SPART, 86 more genes
    nsv6637238copy number variation1nstd102humanPathogenic GRCh37 chr13: 35,501,428-40,901,176 , GRCh38.p12 chr13: 34,927,291-40,327,039 CCDC169-SOHLH2, RNA5SP26, 74 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
    nsv6487779copy number variation1nstd223human GRCh38 chr13: 36,164,582-36,167,388 , GRCh37.p13 chr13: 36,738,719-36,741,525 SOHLH2, CCDC169-SOHLH2
    nsv6487412copy number variation1nstd223human GRCh38 chr13: 36,205,531-36,206,030 , GRCh37.p13 chr13: 36,779,668-36,780,167 SOHLH2, CCDC169-SOHLH2
    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
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6248908mobile element insertion1nstd215human GRCh38 chr13: 36,212,673-36,212,673 , GRCh37.p13 chr13: 36,786,810-36,786,810 SOHLH2, CCDC169-SOHLH2
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6132482copy number variation1nstd213human GRCh37 chr13: 36,710,000-36,880,001 , GRCh38.p12 chr13: 36,135,863-36,305,864 SPART, SOHLH2, 4 more genes
    nsv5971384insertion1nstd209human GRCh38 chr13: 36,184,460-36,184,460 , GRCh37.p13 chr13: 36,758,597-36,758,597 CCDC169-SOHLH2, SOHLH2
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