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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5549779insertion1nstd206human GRCh38 chr13: 42,599,268-42,599,306 , GRCh37.p13 chr13: 43,173,404-43,173,442 TNFSF11
    nsv5146209mobile element insertion1nstd203human GRCh38 chr13: 42,587,721-42,587,732 , GRCh37.p13 chr13: 43,161,857-43,161,868 TNFSF11
    nsv5004527copy number variation1nstd200human GRCh38 chr13: 42,596,869-42,612,689 , GRCh37.p13 chr13: 43,171,005-43,186,825 TNFSF11
    nsv4997187copy number variation1nstd200human GRCh38 chr13: 42,581,454-42,584,101 , GRCh37.p13 chr13: 43,155,590-43,158,237 TNFSF11
    nsv4833500copy number variation1nstd200human GRCh37 chr13: 43,155,590-43,158,237 , GRCh38.p12 chr13: 42,581,454-42,584,101 TNFSF11
    nsv4676076copy number variation1nstd102humanUncertain significance GRCh37 chr13: 43,163,675-43,887,005 , GRCh38.p12 chr13: 42,589,539-43,312,869 LINC01050, LOC107984611, 11 more genes
    nsv4602264copy number variation1nstd183human GRCh37 chr13: 40,306,065-46,460,742 , GRCh38.p12 chr13: 39,731,928-45,886,607 , RN7SKP2, 127 more genes
    nsv4230331copy number variation1nstd166human GRCh37.p13 chr13: 43,159,003-43,161,099 , GRCh38.p12 chr13: 42,584,867-42,586,963 TNFSF11
    nsv4225162copy number variation1nstd166human GRCh37.p13 chr13: 43,138,941-43,139,383 , GRCh38.p12 chr13: 42,564,805-42,565,247 TNFSF11
    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
    nsv3924052copy number variation1nstd102humanPathogenic GRCh38 chr13: 41,288,493-85,137,552 , NCBI36 chr13: 40,760,629-84,609,688 , GRCh37 chr13: 41,862,629-85,711,687 TMEM272, LOC105370241, 535 more genes
    nsv3923911copy number variation1nstd102humanPathogenic GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921 MLNR, SIAH3, 422 more genes
    nsv3923636copy number variation1nstd102humanPathogenic NCBI36 chr13: 37,986,314-50,897,351 , GRCh37 chr13: 39,088,314-51,999,350 , GRCh38 chr13: 38,514,177-51,425,214 TUSC8, SNORA31B, 251 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
    nsv3921404copy number variation1nstd102humanPathogenic GRCh37 chr13: 31,592,297-49,065,340 , GRCh38 chr13: 31,018,160-48,491,204 , NCBI36 chr13: 30,490,297-47,963,341 MIR8079, ZDHHC4P1, 280 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
    nsv3920749copy number variation1nstd102humanPathogenic GRCh37 chr13: 20,407,270-115,064,089 , GRCh38 chr13: 19,833,130-114,298,614 , NCBI36 chr13: 19,305,270-114,082,191 DIAPH3-AS2, LOC105370216, 1281 more genes
    nsv3920039copy number variation2nstd102humanPathogenic GRCh37 chr13: 31,937,609-91,227,546 , NCBI36 chr13: 30,835,609-90,025,547 , GRCh38 chr13: 31,363,472-90,575,292 PSMD10P3, CPB2, 714 more genes
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