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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5698483mobile element insertion1nstd211human GRCh38 chr13: 106,540,341-106,540,341 , GRCh37.p13 chr13: 107,192,689-107,192,689 ARGLU1
    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
    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
    nsv5511088copy number variation1nstd206human GRCh38 chr13: 106,553,857-106,553,908 , GRCh37.p13 chr13: 107,206,205-107,206,256 ARGLU1
    nsv5497062copy number variation1nstd206human GRCh38 chr13: 106,126,808-107,477,062 , GRCh37.p13 chr13: 106,779,157-108,129,410 , RPL35P7, 18 more genes
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv5006850copy number variation1nstd200human GRCh38 chr13: 106,565,356-106,566,478 , GRCh37.p13 chr13: 107,217,704-107,218,826 , ARGLU1
    nsv5006849copy number variation1nstd200human GRCh38 chr13: 106,548,752-106,548,926 , GRCh37.p13 chr13: 107,201,100-107,201,274 ARGLU1
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4834007copy number variation1nstd200human GRCh37 chr13: 107,201,100-107,201,274 , GRCh38.p12 chr13: 106,548,752-106,548,926 ARGLU1
    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
    nsv4675882copy number variation1nstd102humanPathogenic GRCh37 chr13: 104,521,177-109,327,788 , GRCh38.p12 chr13: 103,868,827-108,604,133 LOC107984608, LOC105370353, 39 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
    nsv4615049copy number variation1nstd183human GRCh37 chr13: 107,194,776-107,201,814 , GRCh38.p12 chr13: 106,542,428-106,549,466 ARGLU1
    nsv4607212copy number variation1nstd183human GRCh37 chr13: 107,216,598-107,301,900 , GRCh38.p12 chr13: 106,564,250-106,649,552 , ARGLU1, 1 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
    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
    nsv4455077copy number variation1nstd102humanUncertain significance GRCh37 chr13: 106,041,198-107,581,224 , GRCh38.p12 chr13: 105,388,848-106,928,876 DAOA, PPIAP24, 17 more genes
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