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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148086copy number variation1nstd102humanPathogenic GRCh37 chr10: 124,895,517-135,440,296 , GRCh38.p12 chr10: 123,136,001-133,626,792 FANK1, LOC105378534, 159 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7137208copy number variation1nstd102humanPathogenic GRCh37 chr10: 123,477,898-135,427,143 , GRCh38.p12 chr10: 121,718,384-133,613,639 ZRANB1, LOC105378544, 182 more genes
    nsv7098893copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,610,933-135,439,810 , GRCh38.p12 chr10: 120,851,421-133,626,306 LOC105378571, DOCK1, 196 more genes
    nsv6897209copy number variation1nstd229human GRCh38 chr10: 127,405,577-127,585,426 , GRCh37.p13 chr10: 129,203,841-129,383,690 DOCK1, NPS
    nsv6895852copy number variation1nstd229human GRCh38 chr10: 127,531,907-127,579,747 , GRCh37.p13 chr10: 129,330,171-129,378,011 NPS
    nsv6894777copy number variation1nstd229human GRCh38 chr10: 126,477,130-127,857,950 , GRCh37.p13 chr10: 128,165,699-129,656,214 INSYN2A, LOC105378550, 9 more genes
    nsv6891114copy number variation1nstd229human GRCh38 chr10: 127,305,921-127,902,037 , GRCh37.p13 chr10: 129,104,185-129,700,301 FOXI2, CLRN3, 4 more genes
    nsv6890583copy number variation1nstd229human GRCh38 chr10: 127,522,946-127,552,441 , GRCh37.p13 chr10: 129,321,210-129,350,705 NPS
    nsv6889443copy number variation1nstd229human GRCh38 chr10: 127,241,574-127,877,716 , GRCh37.p13 chr10: 129,039,838-129,675,980 CLRN3, BUB1P1, 4 more genes
    nsv6884703copy number variation1nstd229human GRCh38 chr10: 121,934,615-128,427,106 , GRCh37.p13 chr10: 123,694,130-130,225,370 OAT, C10orf88, 98 more genes
    nsv6878091copy number variation1nstd229human GRCh38 chr10: 127,443,425-127,562,477 , GRCh37.p13 chr10: 129,241,689-129,360,741 DOCK1, NPS
    nsv6638051copy number variation1nstd102humanPathogenic GRCh37 chr10: 128,877,896-131,842,835 , GRCh38.p12 chr10: 127,079,632-130,044,571 AS-PTPRE, MKI67, 23 more genes
    nsv6637863copy number variation1nstd102humanUncertain significance GRCh37 chr10: 128,766,925-129,645,385 , GRCh38.p12 chr10: 126,968,661-127,847,121 LOC105378551, LOC107984059, 5 more genes
    nsv6637817copy number variation1nstd102humanUncertain significance GRCh37 chr10: 129,160,805-129,922,819 , GRCh38.p12 chr10: 127,362,541-128,124,555 DOCK1, FOXI2, 7 more genes
    nsv6637468copy number variation1nstd102humanUncertain significance GRCh37 chr10: 129,298,285-129,812,992 , GRCh38.p12 chr10: 127,500,021-128,014,728 FOXI2, NPS, 3 more genes
    nsv6637456copy number variation1nstd102humanUncertain significance GRCh37 chr10: 126,662,496-133,985,966 , GRCh38.p12 chr10: 124,973,927-132,172,462 LOC107984186, LOC105378550, 82 more genes
    nsv6634415copy number variation1nstd102humanPathogenic GRCh37 chr10: 126,914,469-135,427,143 , GRCh38.p12 chr10: 125,225,900-133,613,639 MGMT, LINC01168, 127 more genes
    nsv6634408copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,198,625-135,427,143 , GRCh38.p12 chr10: 125,510,056-133,613,639 MIR202HG, LOC105378563, 123 more genes
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