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Items: 1 to 20 of 385

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7089537copy number variation1nstd229human GRCh38 chrX: 81,297,715-81,297,928 , GRCh37.p13 chrX: 80,553,214-80,553,427 SH3BGRL
    nsv7089536copy number variation1nstd229human GRCh38 chrX: 81,297,440-81,297,772 , GRCh37.p13 chrX: 80,552,939-80,553,271 SH3BGRL
    nsv7089535copy number variation1nstd229human GRCh38 chrX: 81,297,401-81,305,100 , GRCh37.p13 chrX: 80,552,900-80,560,599 SH3BGRL
    nsv7089534copy number variation1nstd229human GRCh38 chrX: 81,295,289-81,295,453 , GRCh37.p13 chrX: 80,550,788-80,550,952 SH3BGRL
    nsv7089533copy number variation1nstd229human GRCh38 chrX: 81,288,295-81,294,515 , GRCh37.p13 chrX: 80,543,794-80,550,014 SH3BGRL
    nsv7089532copy number variation1nstd229human GRCh38 chrX: 81,263,001-81,283,800 , GRCh37.p13 chrX: 80,518,500-80,539,299 SH3BGRL
    nsv7089531copy number variation1nstd229human GRCh38 chrX: 81,261,901-81,273,700 , GRCh37.p13 chrX: 80,517,400-80,529,199 SH3BGRL
    nsv7089530copy number variation1nstd229human GRCh38 chrX: 81,252,601-81,256,200 , GRCh37.p13 chrX: 80,508,100-80,511,699 SH3BGRL
    nsv7089529copy number variation1nstd229human GRCh38 chrX: 81,247,699-81,247,867 , GRCh37.p13 chrX: 80,503,198-80,503,366 SH3BGRL
    nsv7089528copy number variation1nstd229human GRCh38 chrX: 81,241,848-81,246,597 , GRCh37.p13 chrX: 80,497,347-80,502,096 SH3BGRL
    nsv7089527copy number variation1nstd229human GRCh38 chrX: 81,235,801-81,246,600 , GRCh37.p13 chrX: 80,491,300-80,502,099 SH3BGRL
    nsv7089526copy number variation1nstd229human GRCh38 chrX: 81,235,785-81,241,298 , GRCh37.p13 chrX: 80,491,284-80,496,797 SH3BGRL
    nsv7089525copy number variation1nstd229human GRCh38 chrX: 81,223,648-81,253,133 , GRCh37.p13 chrX: 80,479,147-80,508,632 SH3BGRL
    nsv7089524copy number variation1nstd229human GRCh38 chrX: 81,211,412-81,211,609 , GRCh37.p13 chrX: 80,466,911-80,467,108 SH3BGRL
    nsv7089523copy number variation1nstd229human GRCh38 chrX: 81,210,832-81,222,803 , GRCh37.p13 chrX: 80,466,331-80,478,302 SH3BGRL
    nsv7089517copy number variation1nstd229human GRCh38 chrX: 81,156,073-81,226,956 , GRCh37.p13 chrX: 80,411,572-80,482,455 HMGN5, SH3BGRL
    nsv7089507copy number variation1nstd229human GRCh38 chrX: 81,045,335-81,839,994 , GRCh37.p13 chrX: 80,300,834-81,095,493 LOC105373284, LOC105373285, 4 more genes
    nsv7089457copy number variation1nstd229human GRCh38 chrX: 80,508,685-81,495,723 , GRCh37.p13 chrX: 79,764,184-80,751,222 LOC105373284, WBP11P3, 11 more genes
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