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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
    nsv6112666copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,484,271-149,442,579 , GRCh38.p12 chrX: 140,402,106-150,274,366 MIR508, SPANXN1, 121 more genes
    nsv5975986copy number variation2nstd209human GRCh38 chrX: 141,690,049-141,697,474 , GRCh37.p13 chrX|NW_004070888.1: 785,852-793,277 , GRCh37.p13 chrX: 140,778,210-140,785,631 SPANXD
    nsv5972091copy number variation1nstd209human GRCh38 chrX: 141,697,475-141,721,387 , GRCh37.p13 chrX|NW_004070888.1: 793,278-817,190 , GRCh37.p13 chrX: 140,785,632-140,809,543 SPANXD
    nsv5666147copy number variation1nstd207human GRCh37.p13 chrX|NW_004070888.1: 792,280-792,830 , GRCh38 chrX: 141,696,477-141,697,027 , GRCh37.p13 chrX: 140,784,634-140,785,184 SPANXD
    nsv5432616copy number variation1nstd206human GRCh37.p13 chrX|NW_004070888.1: 676,803-794,303 , GRCh38 chrX: 141,581,000-141,698,500 , GRCh37.p13 chrX: 140,669,121-140,786,657 SPANXA2, SPANXD, 3 more genes
    nsv5423420copy number variation1nstd206human GRCh38 chrX: 141,696,467-141,697,028 , GRCh37.p13 chrX: 140,784,624-140,785,185 , GRCh37.p13 chrX|NW_004070888.1: 792,270-792,831 SPANXD
    nsv5415387copy number variation1nstd206human GRCh37.p13 chrX|NW_004070888.1: 660,903-863,184 , GRCh38 chrX: 141,565,100-141,767,381 , GRCh37.p13 chrX: 140,653,169-140,855,167 SPANXD, SPANXA2-OT1, 3 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
    nsv4909200copy number variation1nstd200human GRCh38 chrX: 141,643,920-141,710,235 , GRCh37.p13 chrX|NW_004070888.1: 739,723-806,038 , GRCh37.p13 chrX: 140,732,051-140,798,391 SPANXD, SPANXA2-OT1
    nsv4782392copy number variation1nstd200human GRCh37 chrX: 140,732,051-140,798,391 , GRCh38.p12 chrX: 141,643,920-141,710,235 SPANXA2-OT1, SPANXD
    nsv4782388copy number variation1nstd200human GRCh37 chrX: 139,997,371-140,939,946 , GRCh38.p12 chrX: 140,915,206-141,852,160 SPANXA1, RNU6-3P, 12 more genes
    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
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4685620copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 122,132,166-155,097,214 , GRCh38.p12 chrX: 122,998,313-155,867,551 ABCD1, AMD1P2, 560 more genes
    nsv4684152copy number variation1nstd102humanUncertain significance GRCh37 chrX: 140,210,323-140,932,981 , GRCh38.p12 chrX: 141,116,138-141,845,195 LDOC1, MAGEC3, 10 more genes
    nsv4680909copy number variation1nstd189human GRCh37.p13 chrX: 140,332,626-140,789,989 , GRCh38.p12 chrX: 141,238,493-141,701,833 SPANXA1, SPANXD, 6 more genes
    nsv4680462copy number variation2nstd189human GRCh37.p13 chrX: 140,330,465-140,786,891 , GRCh38.p12 chrX: 141,236,315-141,698,734 SPANXA1, SPANXD, 6 more genes
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