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Items: 1 to 20 of 158

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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
    nsv6956961copy number variation1nstd229human GRCh38 chr13: 36,731,812-37,044,306 , GRCh37.p13 chr13: 37,305,949-37,618,443 GAPDHP34, SMAD9, 11 more genes
    nsv6952772copy number variation1nstd229human GRCh38 chr13: 36,780,329-36,844,248 , GRCh37.p13 chr13: 37,354,466-37,418,385 LOC102723490, NDE1P2, 3 more genes
    nsv6951403copy number variation1nstd229human GRCh38 chr13: 36,667,941-36,850,506 , GRCh37.p13 chr13: 37,242,078-37,424,643 SERTM1, RFXAP, 6 more genes
    nsv6947065copy number variation1nstd229human GRCh38 chr13: 36,790,960-36,805,804 , GRCh37.p13 chr13: 37,365,097-37,379,941 NDE1P2, ARL2BPP3
    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
    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
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6092154insertion1nstd212human GRCh38 chr13: 36,794,664-36,794,664 , GRCh37.p13 chr13: 37,368,801-37,368,801 ARL2BPP3
    nsv5696432mobile element insertion1nstd211human GRCh38 chr13: 36,794,298-36,794,298 , GRCh37.p13 chr13: 37,368,435-37,368,435 ARL2BPP3
    nsv5656114insertion1nstd207human GRCh38 chr13: 36,794,664-36,794,664 , GRCh37.p13 chr13: 37,368,801-37,368,801 ARL2BPP3
    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
    nsv5430260mobile element insertion1nstd206human GRCh38 chr13: 36,794,298-36,794,341 , GRCh37.p13 chr13: 37,368,435-37,368,478 ARL2BPP3
    nsv5004456copy number variation1nstd200human GRCh38 chr13: 31,196,586-38,438,583 , GRCh37.p13 chr13: 31,770,723-39,012,720 , LOC102723490, 82 more genes
    nsv4761059insertion1nstd199human GRCh37 chr13: 37,368,804-37,368,804 , GRCh38.p12 chr13: 36,794,667-36,794,667 ARL2BPP3
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