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Items: 1 to 20 of 493

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148195copy number variation1nstd102humanPathogenic GRCh37 chr18: 63,476,940-77,960,815 , GRCh38.p12 chr18: 65,809,704-80,202,932 LOC105372202, LINC01896, 149 more genes
    nsv7137214copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,057,406-78,014,123 , GRCh38.p12 chr18: 68,390,169-80,256,240 LOC105372228, MIR548AV, 132 more genes
    nsv7137137copy number variation1nstd102humanPathogenic GRCh37 chr18: 71,740,696-78,005,231 , GRCh38.p12 chr18: 74,073,461-80,247,348 LOC339298, LOC105372201, 84 more genes
    nsv7099035copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,434,850-78,075,000 , GRCh38.p12 chr18: 68,767,613-80,259,271 LOC107985151, CD226, 129 more genes
    nsv7095391copy number variation2nstd102humanUncertain significance GRCh37 chr18: 76,773,973-77,748,392 , GRCh38.p12 chr18: 79,013,973-79,988,392 LOC101927897, LOC107985149, 14 more genes
    nsv7095177copy number variation1nstd102humanUncertain significance GRCh37 chr18: 77,221,291-77,440,281 , GRCh38.p12 chr18: 79,461,291-79,680,281 , GRCh38.p12 chr18|NT_187617.1: 1-122,914 LOC102723506, NFATC1, 6 more genes
    nsv7076010inversion1nstd229human GRCh38 chr18: 76,851,987-80,007,706 , GRCh37.p13 chr18: 74,563,943-77,767,706 SLC66A2, CTDP1-DT, 33 more genes
    nsv7071334inversion1nstd229human GRCh38 chr18: 77,707,319-79,727,290 , GRCh37.p13 chr18: 75,419,275-77,487,290 RNU6-655P, LOC105372224, 20 more genes
    nsv7060951inversion1nstd229human GRCh38 chr18: 76,824,737-79,967,670 , GRCh37.p13 chr18: 74,536,693-77,727,670 CTDP1-DT, KCNG2, 34 more genes
    nsv7016426copy number variation1nstd229human GRCh38 chr18: 79,588,777-79,596,290 , GRCh37.p13 chr18: 77,348,777-77,356,290 LOC284240
    nsv7015623copy number variation1nstd229human GRCh38 chr18: 77,170,889-80,012,828 , GRCh37.p13 chr18: 74,882,845-77,772,828 RNU6-655P, LOC107985171, 29 more genes
    nsv7011395copy number variation1nstd229human GRCh38 chr18: 79,561,461-79,762,262 , GRCh37.p13 chr18: 77,321,461-77,522,262 LOC284240, LOC105372228, 2 more genes
    nsv7008666copy number variation1nstd229human GRCh38 chr18: 79,265,424-80,231,561 , GRCh37.p13 chr18: 77,025,424-77,989,444 CTDP1-DT, SLC66A2, 19 more genes
    nsv7008506copy number variation1nstd229human GRCh38 chr18: 79,577,955-79,582,554 , GRCh37.p13 chr18: 77,337,955-77,342,554 LOC284240
    nsv7006262copy number variation1nstd229human GRCh38 chr18: 79,566,001-79,602,300 , GRCh37.p13 chr18: 77,326,001-77,362,300 LOC284240
    nsv7004207copy number variation1nstd229human GRCh38 chr18: 77,635,799-79,710,878 , GRCh37.p13 chr18: 75,347,755-77,470,878 RNA5SP461, SALL3, 20 more genes
    nsv6998749copy number variation1nstd229human GRCh38 chr18: 79,545,818-80,164,173 , GRCh37.p13 chr18: 77,305,818-77,922,056 CTDP1-DT, SLC66A2, 12 more genes
    nsv6638045copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,530,142-78,014,123 , GRCh38.p12 chr18: 68,862,905-80,256,240 LOC105372211, LOC105372188, 128 more genes
    nsv6638004copy number variation1nstd102humanPathogenic GRCh37 chr18: 61,520,071-78,014,123 , GRCh38.p12 chr18: 63,852,837-80,256,240 LOC107985151, CD226, 165 more genes
    nsv6637467copy number variation1nstd102humanPathogenic GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240 RPL9P31, LOC100422317, 277 more genes
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