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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137759copy number variation1nstd102humanBenign GRCh37 chrX: 135,115,763-135,115,821 , GRCh38 chrX: 136,033,604-136,033,662 SLC9A6
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5883857copy number variation1nstd209human GRCh38 chrX: 136,033,603-136,033,661 , GRCh37.p13 chrX|NW_004070887.1: 964,746-964,804 , GRCh37.p13 chrX: 135,115,762-135,115,820 SLC9A6
    nsv5880695copy number variation1nstd209human GRCh38 chrX: 135,989,856-135,989,932 , GRCh37.p13 chrX|NW_004070887.1: 920,999-921,075 , GRCh37.p13 chrX: 135,072,015-135,072,091 SLC9A6
    nsv5878372copy number variation1nstd209human GRCh38 chrX: 135,974,075-135,974,488 , GRCh37.p13 chrX: 135,056,234-135,056,647 , GRCh37.p13 chrX|NW_004070887.1: 905,218-905,631 SLC9A6, MMGT1
    nsv5719724mobile element insertion1nstd211human GRCh38 chrX: 136,008,589-136,008,589 , GRCh37.p13 chrX: 135,090,748-135,090,748 , GRCh37.p13 chrX|NW_004070887.1: 939,732-939,732 SLC9A6
    nsv5673905copy number variation1nstd102humanPathogenic GRCh37 chrX: 135,104,735-135,106,652 , GRCh38.p12 chrX: 136,022,576-136,024,493 SLC9A6
    nsv5670944copy number variation1nstd207human GRCh37.p13 chrX|NW_004070887.1: 964,746-964,804 , GRCh38 chrX: 136,033,603-136,033,661 , GRCh37.p13 chrX: 135,115,762-135,115,820 SLC9A6
    nsv5426102copy number variation1nstd206human GRCh38 chrX: 136,020,321-136,020,374 , GRCh37.p13 chrX: 135,102,480-135,102,533 , GRCh37.p13 chrX|NW_004070887.1: 951,464-951,517 SLC9A6
    nsv5422287copy number variation1nstd206human GRCh38 chrX: 136,041,515-136,041,574 , GRCh37.p13 chrX: 135,123,674-135,123,733 , GRCh37.p13 chrX|NW_004070887.1: 972,658-972,717 SLC9A6
    nsv5415479copy number variation1nstd206human GRCh38 chrX: 135,974,176-135,974,262 , GRCh37.p13 chrX|NW_004070887.1: 905,319-905,405 , GRCh37.p13 chrX: 135,056,335-135,056,421 SLC9A6, MMGT1
    nsv5381745copy number variation1nstd102humanUncertain significance GRCh37 chrX: 135,080,257-135,292,184 , GRCh38.p12 chrX: 135,998,098-136,210,025 SLC9A6, FHL1, 2 more genes
    nsv5377111translocation1nstd200human GRCh38 chrX: 136,033,662-136,033,662 , GRCh38 chrX: 136,033,606-136,033,606 , GRCh37.p13 chrX|NW_004070887.1: 964,749-964,749 , GRCh37.p13 chrX|NW_004070887.1: 964,805-964,805 , GRCh37.p13 chrX: 135,115,765-135,115,765 , GRCh37.p13 chrX: 135,115,821-135,115,821 SLC9A6
    nsv5193787mobile element insertion1nstd203human GRCh38 chrX: 135,997,765-135,997,785 , GRCh37.p13 chrX: 135,079,924-135,079,944 , GRCh37.p13 chrX|NW_004070887.1: 928,908-928,928 SLC9A6
    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
    nsv4894051copy number variation1nstd200human GRCh38 chrX: 136,003,256-136,007,034 , GRCh37.p13 chrX|NW_004070887.1: 934,399-938,177 , GRCh37.p13 chrX: 135,085,415-135,089,193 SLC9A6
    nsv4894050copy number variation1nstd200human GRCh38 chrX: 135,995,637-135,996,859 , GRCh37.p13 chrX: 135,077,796-135,079,018 , GRCh37.p13 chrX|NW_004070887.1: 926,780-928,002 SLC9A6
    nsv4780506copy number variation1nstd200human GRCh37 chrX: 135,085,717-135,085,772 , GRCh38.p12 chrX: 136,003,558-136,003,613 SLC9A6
    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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