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Items: 1 to 20 of 26631

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3418820copy number variation9nstd162human GRCh38 chr9: 134,262,867-134,262,932 , GRCh37.p13 chr9|NW_004070868.1: 76,491-76,556 , GRCh37.p13 chr9: 137,154,713-137,154,778 0
    nsv3418816insertion8nstd162human GRCh38 chrX: 71,884,995-71,884,995 , GRCh37.p13 chrX: 71,104,845-71,104,845 0
    nsv3418812insertion1nstd162human GRCh38 chrX: 8,169,344-8,169,344 , GRCh37.p13 chrX: 8,137,385-8,137,385 VCX2, LOC107985675
    nsv3418810copy number variation1nstd162human GRCh38 chr8: 1,955,265-1,955,524 , GRCh37.p13 chr8: 1,903,431-1,903,690 ARHGEF10
    nsv3418809insertion3nstd162human GRCh38 chrX: 45,334,612-45,334,612 , GRCh37.p13 chrX: 45,193,857-45,193,857 0
    nsv3418799insertion14nstd162human GRCh38 chr9: 105,887,972-105,887,972 , GRCh37.p13 chr9: 108,650,253-108,650,253 0
    nsv3418793copy number variation1nstd162human GRCh38 chrUn|NT_187443.1: 21,482-21,635 , GRCh37.p13 chr: NaN-NaN 0
    nsv3418791insertion8nstd162human GRCh38 chr7: 157,725,990-157,725,990 , GRCh37.p13 chr7: 157,518,682-157,518,682 PTPRN2
    nsv3418790copy number variation13nstd162human GRCh38 chr9: 66,795,901-66,839,000 , GRCh37.p13 chr9: 66,133,307-66,176,406 CNTNAP3P9
    nsv3418789insertion13nstd162human GRCh38 chr8: 55,911,223-55,911,223 , GRCh37.p13 chr8: 56,823,782-56,823,782 LYN
    nsv3418775insertion12nstd162human GRCh38 chr8: 49,713,404-49,713,404 , GRCh37.p13 chr8: 50,625,964-50,625,964 0
    nsv3418769mobile element insertion13nstd162human GRCh38 chr8: 143,988,243-143,988,243 , GRCh37.p13 chr8|NW_003315923.1: 326,888-326,888 , GRCh37.p13 chr8: 145,062,411-145,062,411 GRINA
    nsv3418749insertion4nstd162human GRCh38 chr7: 158,336,464-158,336,464 , GRCh37.p13 chr7: 158,129,156-158,129,156 PTPRN2
    nsv3418747insertion5nstd162human GRCh38 chr7: 3,977,112-3,977,112 , GRCh37.p13 chr7: 4,016,744-4,016,744 SDK1
    nsv3418745mobile element insertion14nstd162human GRCh38 chr7: 84,299,806-84,299,806 , GRCh37.p13 chr7: 83,929,122-83,929,122 SEMA3A
    nsv3418736insertion11nstd162human GRCh38 chr8: 1,508,512-1,508,512 , GRCh37.p13 chr8: 1,456,678-1,456,678 DLGAP2
    nsv3418734copy number variation3nstd162human GRCh38 chr9: 129,454,046-129,454,127 , GRCh37.p13 chr9: 132,216,325-132,216,406 0
    nsv3418725mobile element insertion2nstd162human GRCh38 chr7: 33,155,706-33,155,706 , GRCh37.p13 chr7: 33,195,318-33,195,318 BBS9
    nsv3418724copy number variation1nstd162human GRCh38 chr8: 1,401,193-1,401,284 , GRCh37.p13 chr8: 1,349,359-1,349,450 DLGAP2
    nsv3418723insertion4nstd162human GRCh38 chr8: 977,718-977,718 , GRCh37.p13 chr8: 927,718-927,718 DLGAP2
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