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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
    nsv5975563copy number variation1nstd209human GRCh38 chrX: 102,772,804-102,776,603 , GRCh37.p13 chrX: 102,027,732-102,031,531 LINC00630, ARMCX5-GPRASP2
    nsv5971725copy number variation1nstd209human GRCh37.p13 chrX: 102,053,958-102,065,392 , GRCh38 chrX: 102,799,030-102,810,464 LINC00630, ARMCX5-GPRASP2, 6 more genes
    nsv5878116copy number variation1nstd209human GRCh38 chrX: 102,834,904-102,835,045 , GRCh37.p13 chrX: 102,089,832-102,089,973 ARMCX5-GPRASP2, LINC00630
    nsv5873727copy number variation1nstd209human GRCh38 chrX: 102,799,442-102,826,581 , GRCh37.p13 chrX: 102,054,370-102,081,509 LINC00630, ARMCX5-GPRASP2, 6 more genes
    nsv5868965copy number variation1nstd209human GRCh38 chrX: 102,773,933-102,777,319 , GRCh37.p13 chrX: 102,028,861-102,032,247 ARMCX5-GPRASP2, LINC00630
    nsv5725474mobile element insertion1nstd211human GRCh38 chrX: 102,922,584-102,922,584 , GRCh37.p13 chrX: 102,177,512-102,177,512 LINC00630
    nsv5604707insertion1nstd207human GRCh38 chrX: 102,785,483-102,785,483 , GRCh37.p13 chrX: 102,040,411-102,040,411 MTND2P2, LINC00630, 2 more genes
    nsv5561316mobile element insertion1nstd206human GRCh38 chrX: 102,922,584-102,922,635 , GRCh37.p13 chrX: 102,177,512-102,177,563 LINC00630
    nsv5543634insertion1nstd206human GRCh38 chrX: 102,851,453-102,851,461 , GRCh37.p13 chrX: 102,106,381-102,106,389 ARMCX5-GPRASP2, LINC00630
    nsv5426040copy number variation1nstd206human GRCh38 chrX: 102,818,372-102,818,439 , GRCh37.p13 chrX: 102,073,300-102,073,367 ARMCX5-GPRASP2, LINC00630
    nsv5376808translocation1nstd200human GRCh38 chrX: 102,801,340-102,801,340 , GRCh38 chrX: 102,880,122-102,880,122 , GRCh37.p13 chrX: 102,056,268-102,056,268 , GRCh37.p13 chrX: 102,135,050-102,135,050 LINC00630, ARMCX5-GPRASP2, 1 more genes
    nsv5376807translocation1nstd200human GRCh38 chrX: 102,826,582-102,826,582 , GRCh38 chrX: 102,799,442-102,799,442 , GRCh37.p13 chrX: 102,054,370-102,054,370 , GRCh37.p13 chrX: 102,081,510-102,081,510 LINC00630, ARMCX5-GPRASP2, 3 more genes
    nsv5376806translocation1nstd200human GRCh38 chrX: 102,788,230-102,788,230 , GRCh38 chrX: 102,882,859-102,882,859 , GRCh37.p13 chrX: 102,137,787-102,137,787 , GRCh37.p13 chrX: 102,043,158-102,043,158 MTND2P2, LINC00630, 1 more genes
    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
    nsv4905821copy number variation1nstd200human GRCh38 chrX: 102,876,648-102,881,981 , GRCh37.p13 chrX: 102,131,576-102,136,909 ARMCX5-GPRASP2, LINC00630
    nsv4905820copy number variation1nstd200human GRCh38 chrX: 102,868,247-102,875,474 , GRCh37.p13 chrX: 102,123,175-102,130,402 LINC00630, ARMCX5-GPRASP2
    nsv4893830copy number variation1nstd200human GRCh38 chrX: 102,858,026-102,868,464 , GRCh37.p13 chrX: 102,112,954-102,123,392 ARMCX5-GPRASP2, LINC00630
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