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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5884342copy number variation1nstd209human GRCh38 chr1: 221,964,560-227,275,238 , GRCh37.p13 chr1: 222,137,902-227,462,939 , YBX1P9, 111 more genes
    nsv5868878copy number variation1nstd209human GRCh38 chr1: 224,009,078-224,009,137 , GRCh37.p13 chr1: 224,196,780-224,196,839 SEPTIN7P13
    nsv5664936inversion1nstd207human GRCh38 chr1: 224,011,799-224,016,559 , GRCh37.p13 chr1: 224,199,501-224,204,261 SEPTIN7P13
    nsv5624416insertion1nstd207human GRCh38 chr1: 224,014,627-224,014,627 , GRCh37.p13 chr1: 224,202,329-224,202,329 SEPTIN7P13
    nsv5623577insertion1nstd207human GRCh38 chr1: 224,012,501-224,012,501 , GRCh37.p13 chr1: 224,200,203-224,200,203 SEPTIN7P13
    nsv5622846insertion1nstd207human GRCh38 chr1: 224,011,844-224,011,844 , GRCh37.p13 chr1: 224,199,546-224,199,546 SEPTIN7P13
    nsv5618297insertion1nstd207human GRCh38 chr1: 224,031,225-224,031,225 , GRCh37.p13 chr1: 224,218,927-224,218,927 SEPTIN7P13
    nsv5614957insertion1nstd207human GRCh38 chr1: 224,013,903-224,013,903 , GRCh37.p13 chr1: 224,201,605-224,201,605 SEPTIN7P13
    nsv5613747insertion1nstd207human GRCh38 chr1: 224,013,772-224,013,772 , GRCh37.p13 chr1: 224,201,474-224,201,474 SEPTIN7P13
    nsv5605913insertion1nstd207human GRCh38 chr1: 224,012,517-224,012,517 , GRCh37.p13 chr1: 224,200,219-224,200,219 SEPTIN7P13
    nsv5577123copy number variation1nstd207human GRCh38 chr1: 224,006,329-224,006,823 , GRCh37.p13 chr1: 224,194,031-224,194,525 SEPTIN7P13
    nsv5576198copy number variation1nstd207human GRCh38 chr1: 223,997,863-224,006,823 , GRCh37.p13 chr1: 224,185,565-224,194,525 SEPTIN7P13
    nsv5570317copy number variation1nstd207human GRCh38 chr1: 224,013,644-224,013,793 , GRCh37.p13 chr1: 224,201,346-224,201,495 SEPTIN7P13
    nsv5568135copy number variation1nstd207human GRCh38 chr1: 224,013,682-224,013,756 , GRCh37.p13 chr1: 224,201,384-224,201,458 SEPTIN7P13
    nsv5567759copy number variation1nstd207human GRCh38 chr1: 224,011,813-224,011,868 , GRCh37.p13 chr1: 224,199,515-224,199,570 SEPTIN7P13
    nsv5453302copy number variation1nstd206human GRCh38 chr1: 223,989,621-223,992,673 , GRCh37.p13 chr1: 224,177,323-224,180,375 SEPTIN7P13, GTF2IP20
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5216499copy number variation1nstd204human GRCh38.p13 chr1: 224,026,501-224,027,100 , GRCh37.p13 chr1: 224,214,203-224,214,802 SEPTIN7P13
    nsv5200338copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,552,998-224,761,890 , GRCh38.p12 chr1: 223,379,656-224,574,188 LOC105373025, CAPN2, 32 more genes
    nsv5068960mobile element insertion1nstd203human GRCh38 chr1: 223,997,738-223,997,754 , GRCh37.p13 chr1: 224,185,440-224,185,456 SEPTIN7P13
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