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Items: 1 to 20 of 136

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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
    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
    nsv6941196copy number variation1nstd229human GRCh38 chr13: 32,439,923-32,660,114 , GRCh37.p13 chr13: 33,014,060-33,234,251 N4BP2L2-IT2, PDS5B-DT, 4 more genes
    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
    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
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 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
    nsv6132478copy number variation1nstd213human GRCh37 chr13: 32,880,000-35,100,001 , GRCh38.p12 chr13: 32,305,863-34,525,864 IFIT1P1, N4BP2L2-IT2, 24 more genes
    nsv6112810copy number variation1nstd102humanPathogenic GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559 MTUS2, ALOX5AP, 70 more genes
    nsv5932755copy number variation1nstd209human GRCh38 chr13: 32,479,616-32,496,966 , GRCh37.p13 chr13: 33,053,753-33,071,103 N4BP2L2, MICOS10P1
    nsv5860585copy number variation1nstd209human GRCh38 chr13: 32,487,550-32,496,776 , GRCh37.p13 chr13: 33,061,687-33,070,913 N4BP2L2, MICOS10P1
    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
    nsv5004460copy number variation1nstd200human GRCh38 chr13: 31,913,588-32,879,794 , GRCh37.p13 chr13: 32,487,725-33,453,932 N4BP2L2, IFIT1P1, 13 more genes
    nsv5004456copy number variation1nstd200human GRCh38 chr13: 31,196,586-38,438,583 , GRCh37.p13 chr13: 31,770,723-39,012,720 , LOC102723490, 82 more genes
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