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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5932776copy number variation1nstd209human GRCh38 chr13: 113,918,469-113,953,043 , GRCh37.p13 chr13: 114,621,442-114,639,948 , LINC00452, 2 more genes
    nsv5856242copy number variation1nstd209human GRCh38 chr13: 113,925,336-113,936,135 , GRCh37.p13 chr13: 114,628,309-114,639,108 , SWINGN
    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
    nsv5503151copy number variation1nstd206human GRCh38 chr13: 113,871,335-114,124,231 , GRCh37.p13 chr13: 114,574,308-114,889,706 , RASA3, 6 more genes
    nsv5275459copy number variation1nstd204human GRCh38.p13 chr13: 113,911,937-113,950,610 , GRCh37.p13 chr13: 114,614,910-114,639,948 , LINC00452, 1 more genes
    nsv5269303copy number variation1nstd204human GRCh38.p13 chr13: 113,775,801-114,100,000 , GRCh37.p13 chr13: 114,478,774-114,865,475 , GAS6, 8 more genes
    nsv5181780mobile element insertion1nstd203human GRCh38 chr13: 113,925,991-113,926,003 , GRCh37.p13 chr13: 114,628,964-114,628,976 SWINGN
    nsv4994033copy number variation1nstd200human GRCh38 chr13: 113,792,082-113,937,362 , GRCh37.p13 chr13: 114,495,055-114,639,948 , GAS6, 6 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
    nsv4729336copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 112,069,981-115,107,733 , GRCh38.p12 chr13: 111,417,634-114,342,258 ATP4B, F7, 68 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
    nsv4633701copy number variation1nstd183human GRCh37 chr13: 114,549,209-114,639,186 , GRCh38.p12 chr13: 113,846,236-113,936,213 , GAS6, 4 more genes
    nsv4530407copy number variation1nstd166human GRCh37.p13 chr13: 114,569,499-114,639,948 , GRCh38.p12 chr13: 113,866,526-113,936,975 , SWINGN, 3 more genes
    nsv4457030copy number variation1nstd102humanPathogenic GRCh37 chr13: 111,568,865-115,107,733 , GRCh38.p12 chr13: 110,916,518-114,342,258 ARHGEF7, LINC00431, 79 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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