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Items: 1 to 20 of 305

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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
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 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
    nsv7052066inversion1nstd229human GRCh38 chr1: 4,379,650-7,782,927 , GRCh37.p13 chr1: 4,439,710-7,842,987 NPHP4, MIR4252, 46 more genes
    nsv7051820inversion1nstd229human GRCh38 chr1: 4,093,135-4,535,140 , GRCh37.p13 chr1: 4,153,195-4,595,200 EEF1DP6, LINC01777, 1 more genes
    nsv6650448copy number variation1nstd229human GRCh38 chr1: 4,417,822-5,034,724 , GRCh37.p13 chr1: 4,477,882-5,094,784 LOC105376674, LINC01777, 4 more genes
    nsv6650443copy number variation1nstd229human GRCh38 chr1: 4,407,467-5,045,120 , GRCh37.p13 chr1: 4,467,527-5,105,180 LINC01646, LOC102724429, 4 more genes
    nsv6650440copy number variation1nstd229human GRCh38 chr1: 4,397,031-4,520,244 , GRCh37.p13 chr1: 4,457,091-4,580,304 LOC105376674, LINC01777
    nsv6650170copy number variation1nstd229human GRCh38 chr1: 4,284,035-4,491,057 , GRCh37.p13 chr1: 4,344,095-4,551,117 LINC01777, LOC105376674
    nsv6650166copy number variation1nstd229human GRCh38 chr1: 4,265,973-4,439,634 , GRCh37.p13 chr1: 4,326,033-4,499,694 LINC01777, LOC105376674
    nsv6649933copy number variation1nstd229human GRCh38 chr1: 4,144,117-4,517,306 , GRCh37.p13 chr1: 4,204,177-4,577,366 LOC105376674, EEF1DP6, 1 more genes
    nsv6649717copy number variation1nstd229human GRCh38 chr1: 4,382,515-4,489,394 , GRCh37.p13 chr1: 4,442,575-4,549,454 LOC105376674, LINC01777
    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
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 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
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