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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098723copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,681,152-107,783,055 , GRCh38.p12 chrX: 108,437,922-108,539,825 COL4A5, COL4A6
    nsv7098484copy number variation1nstd102humanUncertain significance GRCh37 chrX: 107,682,568-107,683,456 , GRCh38.p12 chrX: 108,439,338-108,440,226 COL4A5, COL4A6
    nsv7098210copy number variation1nstd102humanUncertain significance GRCh37 chrX: 107,400,230-107,939,608 , GRCh38.p12 chrX: 108,157,000-108,696,378 COL4A6, COL4A5
    nsv7098107copy number variation1nstd102humanPathogenic GRCh37 chrX: 106,046,084-108,868,249 , GRCh38.p12 chrX: 106,802,854-109,625,020 VSIG1, NXT2, 32 more genes
    nsv7078369copy number variation1nstd229human GRCh38 chrX: 108,429,239-108,433,573 , GRCh37.p13 chrX: 107,672,469-107,676,803 COL4A6
    nsv7078368copy number variation1nstd229human GRCh38 chrX: 108,424,119-108,435,291 , GRCh37.p13 chrX: 107,667,349-107,678,521 COL4A6
    nsv7078367copy number variation1nstd229human GRCh38 chrX: 108,407,614-108,410,192 , GRCh37.p13 chrX: 107,650,844-107,653,422 COL4A6
    nsv7078366copy number variation1nstd229human GRCh38 chrX: 108,407,199-108,491,631 , GRCh37.p13 chrX: 107,650,429-107,734,861 COL4A5, COL4A6
    nsv7078365copy number variation1nstd229human GRCh38 chrX: 108,380,756-108,382,845 , GRCh37.p13 chrX: 107,623,986-107,626,075 COL4A6
    nsv7078364copy number variation1nstd229human GRCh38 chrX: 108,358,578-108,358,741 , GRCh37.p13 chrX: 107,601,808-107,601,971 COL4A6
    nsv7078363copy number variation1nstd229human GRCh38 chrX: 108,354,224-108,356,404 , GRCh37.p13 chrX: 107,597,454-107,599,634 COL4A6
    nsv7078362copy number variation1nstd229human GRCh38 chrX: 108,321,887-108,322,149 , GRCh37.p13 chrX: 107,565,117-107,565,379 COL4A6
    nsv7078361copy number variation1nstd229human GRCh38 chrX: 108,303,601-108,322,700 , GRCh37.p13 chrX: 107,546,831-107,565,930 COL4A6
    nsv7078360copy number variation1nstd229human GRCh38 chrX: 108,286,630-108,294,552 , GRCh37.p13 chrX: 107,529,860-107,537,782 COL4A6
    nsv7078359copy number variation1nstd229human GRCh38 chrX: 108,285,614-108,286,040 , GRCh37.p13 chrX: 107,528,844-107,529,270 COL4A6
    nsv7078358copy number variation1nstd229human GRCh38 chrX: 108,245,729-108,245,911 , GRCh37.p13 chrX: 107,488,959-107,489,141 COL4A6
    nsv7078357copy number variation1nstd229human GRCh38 chrX: 108,241,435-108,248,753 , GRCh37.p13 chrX: 107,484,665-107,491,983 COL4A6
    nsv7078356copy number variation1nstd229human GRCh38 chrX: 108,237,601-108,268,400 , GRCh37.p13 chrX: 107,480,831-107,511,630 COL4A6
    nsv7078355copy number variation1nstd229human GRCh38 chrX: 108,236,095-108,238,242 , GRCh37.p13 chrX: 107,479,325-107,481,472 COL4A6
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