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Items: 1 to 20 of 307

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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
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099174copy number variation1nstd231human GRCh38.p12 chr1: 3,752,749-6,208,083 , GRCh37 chr1: 3,669,313-6,268,143 DFFB, RPL22, 27 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
    nsv6649771copy number variation1nstd229human GRCh38 chr1: 3,903,239-3,908,540 , GRCh37.p13 chr1: 3,819,803-3,823,583 LINC01134
    nsv6649764copy number variation1nstd229human GRCh38 chr1: 3,885,601-3,916,800 , GRCh37.p13 chr1: 3,802,165-3,823,583 C1orf174, LINC01134, 1 more genes
    nsv6649644copy number variation1nstd229human GRCh38 chr1: 3,900,758-3,916,503 , GRCh37.p13 chr1|NW_004070864.2: 1-9,484 , GRCh37.p13 chr1: 3,823,584-3,833,067 C1orf174, LINC01134
    nsv6649643copy number variation1nstd229human GRCh38 chr1: 3,900,516-3,900,623 , GRCh37.p13 chr1: 3,817,080-3,817,187 C1orf174, LINC01134
    nsv6649215copy number variation1nstd229human GRCh38 chr1: 3,532,130-4,419,144 , GRCh37.p13 chr1: 3,448,694-4,479,204 LINC02780, MIR551A, 19 more genes
    nsv6649120copy number variation1nstd229human GRCh38 chr1: 3,906,801-3,909,000 , GRCh37.p13 chr1|NW_004070864.2: 1-1,981 , GRCh37.p13 chr1: 3,823,584-3,825,564 LINC01134
    nsv6648783copy number variation1nstd229human GRCh38 chr1: 3,557,253-4,081,288 , GRCh37.p13 chr1: 3,473,817-4,141,348 LINC02780, MEGF6, 16 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
    nsv6637067copy number variation1nstd102humanUncertain significance GRCh37 chr1: 2,974,212-4,408,415 , GRCh38.p12 chr1: 3,057,648-4,348,355 LRRC47, LOC105378605, 27 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
    nsv6333572copy number variation1nstd223human GRCh38 chr1: 3,900,758-3,916,503 , GRCh37.p13 chr1|NW_004070864.2: 1-9,484 , GRCh37.p13 chr1: 3,823,584-3,833,067 LINC01134, C1orf174
    nsv6318128copy number variation1nstd223human GRCh38 chr1: 3,903,239-3,908,536 , GRCh37.p13 chr1: 3,819,803-3,823,583 LINC01134
    nsv6315409copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746 VAMP3, CTNNBIP1, 245 more genes
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