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Items: 1 to 20 of 509

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv6112681copy number variation1nstd102humanPathogenic GRCh37 chrX: 107,683,053-107,940,795 , GRCh38.p12 chrX: 108,439,823-108,697,565 COL4A6, COL4A5
    nsv5972060copy number variation1nstd209human GRCh38 chrX: 108,322,133-108,326,706 , GRCh37.p13 chrX: 107,565,363-107,569,936 COL4A6
    nsv5715476mobile element insertion1nstd211human GRCh38 chrX: 108,272,701-108,272,701 , GRCh37.p13 chrX: 107,515,931-107,515,931 COL4A6
    nsv5670832copy number variation1nstd207human GRCh38 chrX: 108,364,720-108,379,714 , GRCh37.p13 chrX: 107,607,950-107,622,944 COL4A6
    nsv5555850mobile element insertion1nstd206human GRCh38 chrX: 108,272,701-108,272,752 , GRCh37.p13 chrX: 107,515,931-107,515,982 COL4A6
    nsv5416846copy number variation1nstd206human GRCh38 chrX: 108,416,313-108,416,398 , GRCh37.p13 chrX: 107,659,543-107,659,628 COL4A6
    nsv5415123copy number variation1nstd206human GRCh38 chrX: 108,384,718-108,385,476 , GRCh37.p13 chrX: 107,627,948-107,628,706 COL4A6
    nsv5376859translocation1nstd200human GRCh38 chrX: 108,220,964-108,220,964 , GRCh38 chrX: 108,220,817-108,220,817 , GRCh37.p13 chrX: 107,464,047-107,464,047 , GRCh37.p13 chrX: 107,464,194-107,464,194 COL4A6
    nsv5195715mobile element insertion1nstd203human GRCh38 chrX: 108,272,685-108,272,701 , GRCh37.p13 chrX: 107,515,915-107,515,931 COL4A6
    nsv5168179mobile element insertion1nstd203human GRCh38 chrX: 108,252,308-108,252,324 , GRCh37.p13 chrX: 107,495,538-107,495,554 COL4A6
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905845copy number variation1nstd200human GRCh38 chrX: 108,322,710-108,324,578 , GRCh37.p13 chrX: 107,565,940-107,567,808 COL4A6
    nsv4893866copy number variation1nstd200human GRCh38 chrX: 108,322,738-108,324,560 , GRCh37.p13 chrX: 107,565,968-107,567,790 COL4A6
    nsv4779979copy number variation1nstd200human GRCh37 chrX: 107,631,711-107,634,133 , GRCh38.p12 chrX: 108,388,481-108,390,903 COL4A6
    nsv4779978copy number variation1nstd200human GRCh37 chrX: 107,563,682-107,577,599 , GRCh38.p12 chrX: 108,320,452-108,334,369 COL4A6
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
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