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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940760copy number variation1nstd209human GRCh38 chr13: 45,686,542-45,686,804 , GRCh37.p13 chr13: 46,260,677-46,260,939 LINC01055, AKR1B1P4
    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
    nsv5561330sequence alteration1nstd206human GRCh38 chr13: 44,983,377-49,709,767 , GRCh37.p13 chr13: 45,557,512-50,283,903 , ESD, 103 more genes
    nsv5512369copy number variation1nstd206human GRCh38 chr13: 45,686,546-45,686,805 , GRCh37.p13 chr13: 46,260,681-46,260,940 AKR1B1P4, LINC01055
    nsv5336395translocation1nstd200human GRCh37 chr13: 46,260,681-46,260,681 , GRCh37 chr13: 46,260,940-46,260,940 , GRCh38.p12 chr13: 45,686,546-45,686,546 , GRCh38.p12 chr13: 45,686,805-45,686,805 LINC01055, AKR1B1P4
    nsv5004566copy number variation1nstd200human GRCh38 chr13: 45,659,777-45,793,550 , GRCh37.p13 chr13: 46,233,912-46,367,685 CBY2, SIAH3, 3 more genes
    nsv4997204copy number variation1nstd200human GRCh38 chr13: 43,050,454-56,920,222 , GRCh37.p13 chr13: 43,624,590-57,494,356 , RNY3P2, 222 more genes
    nsv4846242copy number variation1nstd200human GRCh37 chr13: 46,233,912-46,367,685 , GRCh38.p12 chr13: 45,659,777-45,793,550 LINC01055, AKR1B1P4, 3 more genes
    nsv4728809copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 45,487,628-52,639,336 , GRCh38.p12 chr13: 44,913,493-52,065,200 ATP7B, RCBTB2, 155 more genes
    nsv4679126copy number variation1nstd189human GRCh37.p13 chr13: 44,655,843-47,186,905 , GRCh38.p12 chr13: 44,081,707-46,612,770 , CPB2, 69 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
    nsv4218917copy number variation1nstd166human GRCh37.p13 chr13: 46,260,681-46,260,940 , GRCh38.p12 chr13: 45,686,546-45,686,805 AKR1B1P4, LINC01055
    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
    nsv3924173copy number variation1nstd102humanPathogenic GRCh38 chr13: 43,505,396-49,983,668 , NCBI36 chr13: 42,977,532-49,455,805 , GRCh37 chr13: 44,079,532-50,557,804 PCNPP5, LOC105370198, 131 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
    nsv3923642copy number variation1nstd102humanPathogenic GRCh37 chr13: 44,738,887-115,085,141 , NCBI36 chr13: 43,636,887-114,110,750 , GRCh38 chr13: 44,164,751-114,327,173 LOC107984554, HNRNPA1P18, 861 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
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