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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978990inversion1nstd209human GRCh38 chr13: 19,387,175-24,442,537 , GRCh37.p13 chr13: 19,961,315-25,016,675 , PARP4, 111 more genes
    nsv5969193inversion1nstd209human GRCh38 chr13: 19,344,229-24,542,503 , GRCh37.p13 chr13: 19,918,369-25,116,641 , PARP4, 117 more genes
    nsv5930119copy number variation1nstd209human GRCh38 chr13: 19,425,704-24,953,999 , GRCh37.p13 chr13: 19,999,844-25,528,137 , LOC105370102, 128 more genes
    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
    nsv5507635copy number variation1nstd206human GRCh38 chr13: 22,700,106-24,442,106 , GRCh37.p13 chr13: 23,274,245-25,016,244 , SGCG, 40 more genes
    nsv5273316copy number variation1nstd204human GRCh37.p13 chr13: 23,349,440-23,506,139 , GRCh38.p13 chr13: 22,775,301-22,932,000 IPMKP1, BASP1P1, 5 more genes
    nsv5037324inversion1nstd200human GRCh38 chr13: 20,216,099-22,917,425 , GRCh37.p13 chr13: 20,790,238-23,491,564 , BASP1P1, 56 more genes
    nsv4769365copy number variation1nstd102humanUncertain significance GRCh37 chr13: 22,423,865-25,504,992 , GRCh38.p12 chr13: 21,849,726-24,930,854 LOC105370111, DDX39AP1, 63 more genes
    nsv4679122copy number variation1nstd189human GRCh37.p13 chr13: 23,025,543-23,502,767 , GRCh38.p12 chr13: 22,451,404-22,928,628 FTH1P7, IPMKP1, 8 more genes
    nsv4675550copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-24,970,361 , GRCh38.p12 chr13: 18,862,146-24,396,223 MRPL57, TATDN2P3, 129 more genes
    nsv4611052copy number variation1nstd183human GRCh37 chr13: 23,345,384-23,868,510 , GRCh38.p12 chr13: 22,771,245-23,294,371 NUS1P2, TATDN2P3, 13 more genes
    nsv4457197copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,069,228-27,474,401 , GRCh38.p12 chr13: 19,495,088-26,900,264 ZDHHC20, ANKRD20A10P, 154 more genes
    nsv4426876copy number variation1nstd174human GRCh37 chr13: 23,350,255-23,519,918 , GRCh38.p12 chr13: 22,776,116-22,945,779 IPMKP1, BASP1P1, 5 more genes
    nsv4416506copy number variation1nstd174human GRCh37 chr13: 23,331,219-23,990,978 , GRCh38.p12 chr13: 22,757,080-23,416,839 SGCG, IPMKP1, 16 more genes
    nsv4372853copy number variation1nstd173human GRCh37 chr13: 23,154,734-23,657,285 , GRCh38.p12 chr13: 22,580,595-23,083,146 IPMKP1, BASP1P1, 8 more genes
    nsv4215420copy number variation1nstd166human GRCh37.p13 chr13: 23,351,000-23,432,000 , GRCh38.p12 chr13: 22,776,861-22,857,861 IPMKP1, RFESDP1, 1 more genes
    nsv3924676copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,456,040-114,340,285 , GRCh37 chr13: 19,030,180-115,105,760 , NCBI36 chr13: 17,928,180-114,123,862 GRTP1, FABP5P1, 1334 more genes
    nsv3923987copy number variation1nstd102humanLikely benign GRCh37 chr13: 23,338,425-25,018,754 , GRCh38 chr13: 22,764,286-24,444,616 , NCBI36 chr13: 22,236,425-23,916,754 PCOTH, MIR2276, 38 more genes
    nsv3922463copy number variation1nstd102humanPathogenic NCBI36 chr13: 18,418,322-114,088,205 , GRCh37 chr13: 19,520,322-115,070,103 , GRCh38 chr13: 18,946,182-114,304,628 TULP3P1, LOC105370349, 1311 more genes
    nsv3921223copy number variation1nstd102humanPathogenic GRCh38 chr13: 19,671,934-114,340,331 , NCBI36 chr13: 19,144,074-114,123,908 , GRCh37 chr13: 20,246,074-115,085,141 TRIM60P13, LINC00351, 1289 more genes
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