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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099257copy number variation1nstd231human GRCh38.p12 chr1: 203,396,218-207,103,915 , GRCh37 chr1: 203,365,346-207,277,260 ATP2B4, AVPR1B, 116 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7044092inversion1nstd229human GRCh38 chr1: 203,118,726-211,305,271 , GRCh37.p13 chr1: 203,087,854-211,478,613 LOC100420418, LINC00260, 201 more genes
    nsv6674791copy number variation1nstd229human GRCh38 chr1: 203,823,874-203,824,138 , GRCh37.p13 chr1: 203,793,002-203,793,266 ZC3H11A
    nsv6674493copy number variation1nstd229human GRCh38 chr1: 203,804,190-203,806,341 , GRCh37.p13 chr1: 203,773,318-203,775,469 ZC3H11A, LOC100420338
    nsv6667634copy number variation1nstd229human GRCh38 chr1: 203,823,701-203,835,300 , GRCh37.p13 chr1: 203,792,829-203,804,428 ZC3H11A, RPL35AP5
    nsv6666198copy number variation1nstd229human GRCh38 chr1: 203,760,911-203,833,004 , GRCh37.p13 chr1: 203,730,039-203,802,132 ZC3H11A, LOC100420338, 2 more genes
    nsv6664036copy number variation1nstd229human GRCh38 chr1: 203,815,648-203,993,338 , GRCh37.p13 chr1: 203,784,776-203,962,466 CBX1P3, SNRPE, 4 more genes
    nsv6661006copy number variation1nstd229human GRCh38 chr1: 203,839,001-203,894,300 , GRCh37.p13 chr1: 203,808,129-203,863,428 KRT8P29, ZC3H11A, 1 more genes
    nsv6659761copy number variation1nstd229human GRCh38 chr1: 203,821,405-203,824,328 , GRCh37.p13 chr1: 203,790,533-203,793,456 ZC3H11A
    nsv6658622copy number variation1nstd229human GRCh38 chr1: 203,819,117-203,819,162 , GRCh37.p13 chr1: 203,788,245-203,788,290 ZC3H11A
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6550166inversion1nstd223human GRCh38 chr1: 203,809,320-203,809,842 , GRCh37.p13 chr1: 203,778,448-203,778,970 ZC3H11A
    nsv6548735inversion1nstd223human GRCh38 chr1: 203,830,793-203,831,184 , GRCh37.p13 chr1: 203,799,921-203,800,312 ZC3H11A
    nsv6545442inversion1nstd223human GRCh38 chr1: 203,819,560-203,820,224 , GRCh37.p13 chr1: 203,788,688-203,789,352 ZC3H11A
    nsv6545198inversion1nstd223human GRCh38 chr1: 203,837,207-203,837,653 , GRCh37.p13 chr1: 203,806,335-203,806,781 ZC3H11A
    nsv6540779inversion1nstd223human GRCh38 chr1: 203,824,949-203,825,458 , GRCh37.p13 chr1: 203,794,077-203,794,586 ZC3H11A
    nsv6539939inversion1nstd223human GRCh38 chr1: 203,832,258-203,832,977 , GRCh37.p13 chr1: 203,801,386-203,802,105 ZC3H11A
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