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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4662526copy number variation1nstd186human GRCh37 chr1: 13,159,180-13,161,664 , GRCh38.p12 chr1|NT_187517.1: 37,251-39,735 PRAMEF34P
    nsv4661741copy number variation1nstd186human GRCh37 chr1: 13,148,748-13,171,086 , GRCh38.p12 chr1|NT_187517.1: 26,819-49,157 PRAMEF34P, PRAMEF35P
    nsv4661652copy number variation1nstd186human GRCh37 chr1: 13,161,724-13,219,695 , GRCh38.p12 chr1: 13,075,113-13,104,252 , GRCh38.p12 chr1: 13,104,253-13,152,244 , GRCh38.p12 chr1: 13,122,522-13,166,717 , GRCh38.p12 chr1|NT_187517.1: 49,792-97,838 , GRCh38.p12 chr1|NW_012132914.1: 214,415-258,592 , GRCh38.p12 chr1|NW_012132914.1: 258,593-306,584 , GRCh38.p12 chr1|NW_015495298.1: 55,691-99,868 , GRCh38.p12 chr1|NW_015495298.1: 99,869-147,860 HNRNPCL2, PRAMEF25, 6 more genes
    nsv4660015copy number variation1nstd186human GRCh37 chr1: 13,132,173-13,215,470 , GRCh38.p12 chr1: 13,122,522-13,166,717 , GRCh38.p12 chr1|NT_187517.1: 49,792-93,612 , GRCh38.p12 chr1|NW_012132914.1: 214,415-258,592 , GRCh38.p12 chr1|NW_012132914.1: 258,593-302,359 , GRCh38.p12 chr1|NW_015495298.1: 55,691-99,868 , GRCh38.p12 chr1|NW_015495298.1: 99,869-143,635 HNRNPCL2, PRAMEF25, 6 more genes
    nsv4656633copy number variation3nstd186human GRCh37 chr1: 13,121,600-13,143,100 , GRCh38.p12 chr1|NT_187517.1: 1-21,171 , LOC100132865
    nsv4656049copy number variation1nstd186human GRCh37 chr1: 13,156,000-13,161,100 , GRCh38.p12 chr1|NT_187517.1: 34,071-39,171 PRAMEF34P
    nsv4655610copy number variation1nstd186human GRCh37 chr1: 13,145,500-13,178,000 , GRCh38.p12 chr1|NT_187517.1: 23,571-49,791 , PRAMEF34P, 1 more genes
    nsv4652622copy number variation4nstd186human GRCh37 chr1: 13,145,500-13,152,000 , GRCh38.p12 chr1|NT_187517.1: 23,571-30,071
    nsv4651334copy number variation1nstd186human GRCh37 chr1: 13,164,000-13,172,000 , GRCh38.p12 chr1|NT_187517.1: 42,071-49,791 PRAMEF35P, PRAMEF34P
    nsv4645436copy number variation1nstd186human GRCh37 chr1: 13,155,000-13,197,000 , GRCh38.p12 chr1: 13,122,522-13,166,717 , GRCh38.p12 chr1|NT_187517.1: 49,792-75,092 , GRCh38.p12 chr1|NW_012132914.1: 258,593-283,888 , GRCh38.p12 chr1|NW_012132914.1: 214,415-258,592 , GRCh38.p12 chr1|NW_015495298.1: 99,869-125,164 , GRCh38.p12 chr1|NW_015495298.1: 55,691-99,868 HNRNPCL2, PRAMEF25, 6 more genes
    nsv4642497copy number variation1nstd186human GRCh37 chr1: 13,113,200-13,146,000 , GRCh38.p12 chr1|NT_187517.1: 1-24,071 , LOC100132865
    nsv4639736copy number variation1nstd186human GRCh37 chr1: 13,145,450-13,216,000 , GRCh38.p12 chr1: 13,122,522-13,166,717 , GRCh38.p12 chr1|NT_187517.1: 49,792-94,142 , GRCh38.p12 chr1|NW_012132914.1: 258,593-302,889 , GRCh38.p12 chr1|NW_012132914.1: 214,415-258,592 , GRCh38.p12 chr1|NW_015495298.1: 99,869-144,165 , GRCh38.p12 chr1|NW_015495298.1: 55,691-99,868 HNRNPCL2, PRAMEF25, 6 more genes
    nsv4638564copy number variation4nstd186human GRCh37 chr1: 13,158,400-13,165,000 , GRCh38.p12 chr1|NT_187517.1: 36,471-43,071 PRAMEF34P
    nsv4593867copy number variation2nstd183human GRCh37 chr1: 13,103,193-13,145,660 , GRCh38.p12 chr1|NT_187517.1: 1-23,731 , LOC100132865
    nsv4579327copy number variation1nstd183human GRCh37 chr1: 13,657,869-13,696,620 , GRCh38.p12 chr1: 13,190,999-13,217,064 , GRCh38.p12 chr1: 13,011,883-13,037,941 , GRCh38.p12 chr1|NT_187517.1: 134,415-160,528 , GRCh38.p12 chr1|NW_012132914.1: 345,312-371,404 , GRCh38.p12 chr1|NW_015495298.1: 7,283-33,557 , GRCh38.p12 chr1|NW_012132914.1: 166,234-192,281 LOC107987483, PRAMEF13, 1 more genes
    nsv4579320copy number variation1nstd183human GRCh37 chr1: 13,412,434-13,472,244 , GRCh38.p12 chr1: 13,327,497-13,366,622 , GRCh38.p12 chr1|NT_187517.1: 160,680-256,271 , GRCh38.p12 chr1|NW_012132914.1: 371,405-467,143 PRAMEF5, PRAMEF8, 7 more genes
    nsv4579316copy number variation1nstd183human GRCh37 chr1: 13,219,346-13,435,984 , GRCh38.p12 chr1|NT_187517.1: 97,489-256,271 , GRCh38.p12 chr1|NW_012132914.1: 306,235-467,143 PRAMEF31P, RNU6-771P, 9 more genes
    nsv4579313copy number variation1nstd183human GRCh37 chr1: 13,161,724-13,219,695 , GRCh38.p12 chr1: 13,122,522-13,166,717 , GRCh38.p12 chr1: 13,104,253-13,152,244 , GRCh38.p12 chr1: 13,075,113-13,104,252 , GRCh38.p12 chr1|NT_187517.1: 49,792-97,838 , GRCh38.p12 chr1|NW_012132914.1: 258,593-306,584 , GRCh38.p12 chr1|NW_012132914.1: 214,415-258,592 , GRCh38.p12 chr1|NW_015495298.1: 55,691-99,868 , GRCh38.p12 chr1|NW_015495298.1: 99,869-147,860 HNRNPCL2, PRAMEF25, 6 more genes
    nsv4579312copy number variation2nstd183human GRCh37 chr1: 13,159,180-13,161,664 , GRCh38.p12 chr1|NT_187517.1: 37,251-39,735 PRAMEF34P
    nsv4579311copy number variation1nstd183human GRCh37 chr1: 13,151,732-13,161,381 , GRCh38.p12 chr1|NT_187517.1: 29,803-39,452 PRAMEF34P
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