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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094474copy number variation1nstd102humanPathogenic GRCh37 chr13: 32,906,389-32,972,907 , GRCh38.p12 chr13: 32,332,252-32,398,770 N4BP2L1, BRCA2, 1 more genes
    nsv7094074copy number variation1nstd102humanPathogenic GRCh37 chr13: 32,944,519-32,972,907 , GRCh38.p12 chr13: 32,370,382-32,398,770 N4BP2L1, BRCA2, 1 more genes
    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
    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
    nsv7068176inversion1nstd229human GRCh38 chr13: 30,840,951-32,715,747 , GRCh37.p13 chr13: 31,415,088-33,289,884 MEDAG, N4BP2L1, 25 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
    nsv6956784copy number variation1nstd229human GRCh38 chr13: 32,427,527-32,430,749 , GRCh37.p13 chr13: 33,001,664-33,004,886 N4BP2L2, N4BP2L1
    nsv6953020copy number variation1nstd229human GRCh38 chr13: 32,429,233-32,432,987 , GRCh37.p13 chr13: 33,003,370-33,007,124 N4BP2L2, N4BP2L1
    nsv6942334copy number variation1nstd229human GRCh38 chr13: 32,428,342-32,436,035 , GRCh37.p13 chr13: 33,002,479-33,010,172 N4BP2L2, N4BP2L1
    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
    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
    nsv6592259inversion1nstd223human GRCh38 chr13: 32,405,270-32,405,924 , GRCh37.p13 chr13: 32,979,407-32,980,061 N4BP2L1
    nsv6482873copy number variation1nstd223human GRCh38 chr13: 32,413,270-32,414,792 , GRCh37.p13 chr13: 32,987,407-32,988,929 N4BP2L1
    nsv6480989copy number variation1nstd223human GRCh38 chr13: 32,428,341-32,436,034 , GRCh37.p13 chr13: 33,002,478-33,010,171 N4BP2L1, N4BP2L2
    nsv6480598copy number variation1nstd223human GRCh38 chr13: 32,408,592-32,409,595 , GRCh37.p13 chr13: 32,982,729-32,983,732 N4BP2L1
    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
    nsv6309680copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr13: 32,953,434-32,972,907 , GRCh38.p12 chr13: 32,379,297-32,398,770 BRCA2, IFIT1P1, 1 more genes
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