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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5708558mobile element insertion2nstd211human GRCh38 chr13: 60,787,895-60,787,895 , GRCh37.p13 chr13: 61,362,029-61,362,029 RNY3P5, LINC01442
    nsv5585678copy number variation1nstd207human GRCh38 chr13: 60,787,866-60,787,963 , GRCh37.p13 chr13: 61,362,000-61,362,097 LINC01442, RNY3P5
    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
    nsv5422022mobile element insertion1nstd206human GRCh38 chr13: 60,787,895-60,787,946 , GRCh37.p13 chr13: 61,362,029-61,362,080 RNY3P5, LINC01442
    nsv5141777mobile element insertion1nstd203human GRCh38 chr13: 60,787,880-60,787,890 , GRCh37.p13 chr13: 61,362,014-61,362,024 RNY3P5, LINC01442
    nsv5034873inversion1nstd200human GRCh38 chr13: 55,150,893-76,780,363 , GRCh37.p13 chr13: 55,725,028-77,354,498 , PRR20C, 199 more genes
    nsv4872325inversion1nstd200human GRCh37 chr13: 55,725,028-77,354,498 , GRCh38.p12 chr13: 55,150,893-76,780,363 , OR7E111P, 199 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
    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
    nsv4603750copy number variation1nstd183human GRCh37 chr13: 61,311,481-61,395,919 , GRCh38.p12 chr13: 60,737,347-60,821,785 RNY3P5, RNY4P31, 1 more genes
    nsv4436742copy number variation1nstd102humanUncertain significance GRCh37 chr13: 54,638,436-63,254,336 , GRCh38.p12 chr13: 54,064,301-62,680,203 RPL13AP25, LINC00434, 69 more genes
    nsv4424054copy number variation1nstd174human GRCh37 chr13: 61,319,533-61,395,907 , GRCh38.p12 chr13: 60,745,399-60,821,773 RNY4P31, LINC01442, 1 more genes
    nsv4349132copy number variation1nstd102humanPathogenic GRCh37 chr13: 59,424,409-65,723,208 , GRCh38.p12 chr13: 58,850,275-65,149,076 LINC01074, LOC105370237, 59 more genes
    nsv4217161copy number variation1nstd166human GRCh37.p13 chr13: 61,290,416-61,379,730 , GRCh38.p12 chr13: 60,716,282-60,805,596 LINC01442, RNY3P5
    nsv4216710copy number variation1nstd166human GRCh37.p13 chr13: 61,318,000-61,402,000 , GRCh38.p12 chr13: 60,743,866-60,827,866 LINC01442, RNY4P31, 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
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3924346copy number variation1nstd102humanLikely benign GRCh38 chr13: 60,049,295-60,879,301 , GRCh37 chr13: 60,623,429-61,453,435 , NCBI36 chr13: 59,521,430-60,351,436 LOC105370230, LOC105370227, 13 more genes
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