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Items: 1 to 20 of 366

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5880133copy number variation1nstd209human GRCh38 chrX: 19,919,612-19,920,710 , GRCh37.p13 chrX: 19,937,730-19,938,828 BCLAF3
    nsv5423564copy number variation1nstd206human GRCh38 chrX: 19,910,785-19,910,872 , GRCh37.p13 chrX: 19,928,903-19,928,990 BCLAF3
    nsv5421347copy number variation1nstd206human GRCh38 chrX: 19,928,421-19,930,152 , GRCh37.p13 chrX: 19,946,539-19,948,270 BCLAF3
    nsv5420032copy number variation1nstd206human GRCh38 chrX: 19,926,924-19,928,330 , GRCh37.p13 chrX: 19,945,042-19,946,448 BCLAF3
    nsv5415145copy number variation1nstd206human GRCh38 chrX: 19,910,247-19,911,278 , GRCh37.p13 chrX: 19,928,365-19,929,396 BCLAF3
    nsv5381747copy number variation5nstd102humanUncertain significance GRCh37 chrX: 17,393,881-20,284,750 , GRCh38.p12 chrX: 17,375,758-20,266,632 TMSB10P2, BLOC1S6P1, 37 more genes
    nsv5367887translocation1nstd200human GRCh38 chrX: 19,937,009-19,937,009 , GRCh38 chr4: 186,136,511-186,136,511 , GRCh37.p13 chr4: 187,057,665-187,057,665 , GRCh37.p13 chrX: 19,955,127-19,955,127 FAM149A, BCLAF3
    nsv5366446translocation1nstd200human GRCh38 chrX: 19,977,152-19,977,152 , GRCh38 chrX: 19,977,220-19,977,220 , GRCh37.p13 chrX: 19,995,270-19,995,270 , GRCh37.p13 chrX: 19,995,338-19,995,338 BCLAF3
    nsv5200361copy number variation1nstd102humanPathogenic GRCh37 chrX: 19,183,657-20,215,858 , GRCh38.p12 chrX: 19,165,539-20,197,740 EIF5P2, SH3KBP1, 10 more genes
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv4905243copy number variation1nstd200human GRCh38 chrX: 19,965,931-20,169,132 , GRCh37.p13 chrX: 19,984,049-20,187,250 EIF1AX, MIR23C, 6 more genes
    nsv4905242copy number variation1nstd200human GRCh38 chrX: 19,957,246-20,243,041 , GRCh37.p13 chrX: 19,975,364-20,261,159 EIF1AX, LOC729609, 6 more genes
    nsv4905240copy number variation1nstd200human GRCh38 chrX: 19,643,477-19,929,842 , GRCh37.p13 chrX: 19,661,595-19,947,960 SH3KBP1, BCLAF3
    nsv4893759copy number variation1nstd200human GRCh38 chrX: 19,938,139-19,939,075 , GRCh37.p13 chrX: 19,956,257-19,957,193 BCLAF3
    nsv4893758copy number variation1nstd200human GRCh38 chrX: 19,910,785-19,910,872 , GRCh37.p13 chrX: 19,928,903-19,928,990 BCLAF3
    nsv4779240copy number variation1nstd200human GRCh37 chrX: 20,003,212-20,009,409 , GRCh38.p12 chrX: 19,985,094-19,991,291 LOC729609, BCLAF3
    nsv4772531copy number variation1nstd200human GRCh37 chrX: 19,984,049-20,187,250 , GRCh38.p12 chrX: 19,965,931-20,169,132 MIR23C, EIF1AX, 6 more genes
    nsv4769248copy number variation1nstd201human GRCh37 chrX: 168,546-21,870,371 , GRCh38.p12 chrX: 251,879-21,852,253 , AMELX, 248 more genes
    nsv4728625copy number variation1nstd102humanUncertain significance GRCh37 chrX: 20,007,752-20,498,564 , GRCh38.p12 chrX: 19,989,634-20,480,446 EIF1AX-AS1, EIF1AX, 7 more genes
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