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Items: 1 to 20 of 199

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5971876insertion1nstd209human GRCh38 chr13: 110,813,129-110,813,129 , GRCh37.p13 chr13: 111,465,476-111,465,476 LINC00567, LOC105370362
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5604360copy number variation1nstd207human GRCh38 chr13: 110,813,041-110,813,216 , GRCh37.p13 chr13: 111,465,388-111,465,563 LINC00567, LOC105370362
    nsv5594486copy number variation1nstd207human GRCh38 chr13: 110,813,539-110,813,610 , GRCh37.p13 chr13: 111,465,886-111,465,957 LOC105370362, LINC00567
    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
    nsv5553073insertion1nstd206human GRCh38 chr13: 110,813,154-110,813,180 , GRCh37.p13 chr13: 111,465,501-111,465,527 LINC00567, LOC105370362
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv5006998copy number variation1nstd200human GRCh38 chr13: 110,807,702-110,809,491 , GRCh37.p13 chr13: 111,460,049-111,461,838 LINC00567
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4769247copy number variation1nstd201human GRCh37 chr13: 109,490,236-115,107,733 , GRCh38.p12 chr13: 108,837,888-114,342,258 , PARP1P1, 117 more genes
    nsv4753161insertion1nstd199human GRCh37 chr13: 111,465,570-111,465,570 , GRCh38.p12 chr13: 110,813,223-110,813,223 LINC00567, LOC105370362
    nsv4729392copy number variation1nstd102humanUncertain significance GRCh37 chr13: 111,374,280-112,537,874 , GRCh38.p12 chr13: 110,721,933-111,883,560 PRECSIT, LOC107983958, 23 more genes
    nsv4729275copy number variation1nstd102humanUncertain significance GRCh37 chr13: 109,752,674-112,352,804 , GRCh38.p12 chr13: 109,100,326-111,700,457 ANKRD10, CARS2, 46 more genes
    nsv4728884copy number variation1nstd102humanPathogenic GRCh37 chr13: 106,256,198-115,107,733 , GRCh38.p12 chr13: 105,603,849-114,342,258 LINC01044, CARS2, 139 more genes
    nsv4728419copy number variation1nstd102humanPathogenic GRCh37 chr13: 102,175,801-115,169,858 , GRCh38.p12 chr13: 101,523,450-114,344,403 RPL7P45, LOC107984615, 182 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
    nsv4675644copy number variation1nstd102humanPathogenic GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258 ZIC2, LINC03032, 266 more genes
    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
    nsv4456505copy number variation1nstd102humanUncertain significance GRCh37 chr13: 109,203,109-115,107,733 , GRCh38.p12 chr13: 108,550,761-114,342,258 LINC01054, GAS6-DT, 111 more genes
    nsv4456260copy number variation1nstd102humanUncertain significance GRCh37 chr13: 94,849,303-115,107,733 , GRCh38.p12 chr13: 94,197,049-114,342,258 F10, FKSG29, 300 more genes
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