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Items: 1 to 20 of 442

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137191copy number variation1nstd102humanPathogenic GRCh37 chr1: 1,957,148-6,553,454 , GRCh38.p12 chr1: 2,025,709-6,493,394 LOC102724429, TNFRSF14, 86 more genes
    nsv7137068copy number variation1nstd102humanLikely benign GRCh37 chr1: 2,567,832-3,209,952 , GRCh38.p12 chr1: 2,636,393-3,293,388 PRDM16, LOC107984904, 16 more genes
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7098948copy number variation1nstd102humanUncertain significance GRCh38 chr1: 2,518,272-4,413,203 , GRCh37.p13 chr1: 2,449,711-4,473,263 LOC107984904, DFFB, 46 more genes
    nsv7058041inversion1nstd229human GRCh38 chr1: 1,845,355-9,534,096 , GRCh37.p13 chr1: 1,776,794-9,594,155 RPL37P9, TMEM52, 152 more genes
    nsv7054534inversion1nstd229human GRCh38 chr1: 2,972,403-10,562,308 , GRCh37.p13 chr1: 2,888,967-10,622,365 RN7SL731P, LOC105376682, 145 more genes
    nsv7051203inversion1nstd229human GRCh38 chr1: 2,476,867-3,696,891 , GRCh37.p13 chr1: 2,408,306-3,613,455 TP73, PRXL2B, 33 more genes
    nsv6648440copy number variation1nstd229human GRCh38 chr1: 3,004,990-3,396,785 , GRCh37.p13 chr1: 2,921,554-3,313,349 LOC105378604, PRDM16, 7 more genes
    nsv6648398copy number variation1nstd229human GRCh38 chr1: 3,017,666-3,019,973 , GRCh37.p13 chr1: 2,934,230-2,936,537 ACTRT2
    nsv6648386copy number variation1nstd229human GRCh38 chr1: 2,999,698-3,124,285 , GRCh37.p13 chr1: 2,916,262-3,040,849 PRDM16, LOC100420339, 2 more genes
    nsv6647946copy number variation1nstd229human GRCh38 chr1: 2,998,246-3,073,575 , GRCh37.p13 chr1: 2,914,810-2,990,139 PRDM16-DT, LOC100420339, 2 more genes
    nsv6647889copy number variation1nstd229human GRCh38 chr1: 2,849,299-3,028,520 , GRCh37.p13 chr1: 2,765,864-2,945,084 ACTRT2
    nsv6647879copy number variation1nstd229human GRCh38 chr1: 2,800,201-3,815,100 , GRCh37.p13 chr1: 2,716,766-3,731,664 CEP104, PRDM16-DT, 22 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6636594copy number variation1nstd102humanUncertain significance GRCh37 chr1: 2,628,158-3,191,234 , GRCh38.p12 chr1: 2,696,719-3,274,670 PRDM16, LOC105378599, 15 more genes
    nsv6636460copy number variation1nstd102humanUncertain significance GRCh37 chr1: 2,621,577-3,021,311 , GRCh38.p12 chr1: 2,690,138-3,104,747 ACTRT2, LOC105378600, 11 more genes
    nsv6636408copy number variation1nstd102humanUncertain significance GRCh37 chr1: 2,194,087-4,738,355 , GRCh38.p12 chr1: 2,262,648-4,678,295 LINC01777, LOC105378606, 55 more genes
    nsv6636399copy number variation1nstd102humanPathogenic GRCh37 chr1: 2,173,570-5,023,430 , GRCh38.p12 chr1: 2,242,131-4,963,370 LOC105378602, MORN1, 55 more genes
    nsv6636292copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-2,972,435 , GRCh38.p12 chr1: 914,087-3,055,871 LOC105378602, LOC105378599, 108 more genes
    nsv6635519copy number variation1nstd227human GRCh38.p12 chr1: 2,783,827-3,291,811 , GRCh37 chr1: 2,700,372-3,208,375 PRDM16, ACTRT2, 8 more genes
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