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Items: 1 to 20 of 165

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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
    nsv6955062copy number variation1nstd229human GRCh38 chr13: 37,466,539-37,599,987 , GRCh37.p13 chr13: 38,040,676-38,174,124 POSTN, LINC01048, 1 more genes
    nsv6948889copy number variation1nstd229human GRCh38 chr13: 37,462,801-37,494,100 , GRCh37.p13 chr13: 38,036,938-38,068,237 LINC01048
    nsv6942370copy number variation1nstd229human GRCh38 chr13: 37,460,406-37,561,471 , GRCh37.p13 chr13: 38,034,543-38,135,608 LINC00547, POSTN, 1 more genes
    nsv6941462copy number variation1nstd229human GRCh38 chr13: 37,462,701-37,495,700 , GRCh37.p13 chr13: 38,036,838-38,069,837 LINC01048
    nsv6941266copy number variation1nstd229human GRCh38 chr13: 37,478,372-37,535,064 , GRCh37.p13 chr13: 38,052,509-38,109,201 LINC00547, LINC01048
    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
    nsv6488835copy number variation1nstd223human GRCh38 chr13: 37,480,293-37,481,783 , GRCh37.p13 chr13: 38,054,430-38,055,920 LINC01048
    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
    nsv6291701copy number variation1nstd102humanUncertain significance GRCh37 chr13: 37,464,566-38,493,263 , GRCh38.p12 chr13: 36,890,429-37,919,126 LINC00547, ALG5, 14 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
    nsv6132643copy number variation1nstd213human GRCh37 chr13: 38,010,000-38,490,001 , GRCh38.p12 chr13: 37,435,863-37,915,864 TRPC4, POSTN, 3 more genes
    nsv6132642copy number variation1nstd213human GRCh37 chr13: 37,950,000-38,870,001 , GRCh38.p12 chr13: 37,375,863-38,295,864 TRPC4, POSTN, 6 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
    nsv5851396copy number variation1nstd209human GRCh38 chr13: 37,481,584-37,482,683 , GRCh37.p13 chr13: 38,055,721-38,056,820 LINC01048
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
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