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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
    nsv5857451copy number variation1nstd209human GRCh38 chr13: 64,440,446-64,441,645 , GRCh37.p13 chr13: 65,014,578-65,015,777 LOC105370238
    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
    nsv5502560copy number variation1nstd206human GRCh38 chr13: 63,817,163-65,941,403 , GRCh37.p13 chr13: 64,391,296-66,515,535 LGMNP1, OR7E104P, 15 more genes
    nsv5262713copy number variation1nstd204human GRCh38.p13 chr13: 64,447,501-64,452,400 , GRCh37.p13 chr13: 65,021,633-65,026,532 LOC105370238
    nsv5039398inversion1nstd200human GRCh38 chr13: 63,499,867-68,921,282 , GRCh37.p13 chr13: 64,074,000-69,495,414 RN7SL761P, STARP1, 55 more genes
    nsv5034873inversion1nstd200human GRCh38 chr13: 55,150,893-76,780,363 , GRCh37.p13 chr13: 55,725,028-77,354,498 , PRR20C, 199 more genes
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv5032796inversion1nstd200human GRCh38 chr13: 64,003,818-65,380,883 , GRCh37.p13 chr13: 64,577,951-65,955,015 STARP1, LGMNP1, 5 more genes
    nsv4872325inversion1nstd200human GRCh37 chr13: 55,725,028-77,354,498 , GRCh38.p12 chr13: 55,150,893-76,780,363 , OR7E111P, 199 more genes
    nsv4871291inversion1nstd200human GRCh37 chr13: 64,074,000-69,495,413 , GRCh38.p12 chr13: 63,499,867-68,921,281 NFYAP1, RN7SL761P, 55 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4680105copy number variation1nstd189human GRCh37.p13 chr13: 58,938,513-65,829,014 , GRCh38.p12 chr13: 58,364,379-65,254,882 , PCDH20, 66 more genes
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675752copy number variation1nstd102humanLikely benign GRCh37 chr13: 63,995,811-65,490,454 , GRCh38.p12 chr13: 63,421,678-64,916,322 LOC105370239, LOC105370236, 16 more genes
    nsv4675016copy number variation1nstd102humanUncertain significance GRCh37 chr13: 58,432,035-73,649,333 , GRCh38.p12 chr13: 57,857,901-73,075,195 TRIM60P19, ATXN8OS, 137 more genes
    nsv4530180copy number variation1nstd166human GRCh37.p13 chr13: 64,415,999-65,368,000 , GRCh38.p12 chr13: 63,841,866-64,793,868 LINC00355, NFYAP1, 6 more genes
    nsv4508793mobile element insertion1nstd166human GRCh37.p13 chr13: 65,009,825-65,009,825 , GRCh38.p12 chr13: 64,435,693-64,435,693 LOC105370238
    nsv4456561copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,775,567-115,107,733 , GRCh38.p12 chr13: 61,201,433-114,342,258 LOC105370262, LINC01080, 609 more genes
    nsv4455111copy number variation1nstd102humanUncertain significance GRCh37 chr13: 62,153,364-67,984,114 , GRCh38.p12 chr13: 61,579,231-67,409,982 LOC105370232, LOC105370238, 47 more genes
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