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Items: 1 to 20 of 598

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4680613copy number variation1nstd189human GRCh37.p13 chrX: 124,460,560-125,042,054 , GRCh38.p12 chrX: 125,326,711-125,908,072 FBLIM1P1
    nsv4680366copy number variation1nstd189human GRCh38.p12 chr2: 225,897,611-226,398,125 , GRCh37.p13 chr2: 226,762,327-227,262,841 LOC646736
    nsv4680373copy number variation1nstd189human GRCh38.p12 chr10: 66,321,054-66,750,843 , GRCh37.p13 chr10: 68,080,812-68,510,601 CTNNA3
    nsv4680718copy number variation1nstd189human GRCh37.p13 chrX: 31,547,597-31,950,715 , GRCh38.p12 chrX: 31,529,480-31,932,598 DMD
    nsv4680375copy number variation1nstd189human GRCh37.p13 chr11: 96,274,784-96,809,830 , GRCh38.p12 chr11: 96,541,620-96,938,830 AKTIPP3
    nsv4679071copy number variation1nstd189human GRCh37.p13 chr7: 125,472,700-125,839,542 , GRCh38.p12 chr7: 125,832,646-126,199,488 LOC105375487
    nsv4679318copy number variation1nstd189human GRCh38.p12 chr9: 11,224,343-11,586,197 , GRCh37.p13 chr9: 11,224,343-11,586,197 LOC105375974
    nsv4679291copy number variation1nstd189human GRCh37.p13 chr7: 146,419,360-146,762,872 , GRCh38.p12 chr7: 146,722,268-147,065,780 CNTNAP2
    nsv4679763copy number variation1nstd189human GRCh37.p13 chr7: 146,424,882-146,764,997 , GRCh38.p12 chr7: 146,727,790-147,067,905 CNTNAP2
    nsv4679755copy number variation1nstd189human GRCh38.p12 chr1: 189,255,744-189,578,508 , GRCh37.p13 chr1: 189,224,875-189,547,638 LOC105371657
    nsv4680072copy number variation1nstd189human GRCh38.p12 chr10: 55,104,168-55,416,187 , GRCh37.p13 chr10: 56,863,928-57,175,947 PCDH15
    nsv4680773copy number variation1nstd189human GRCh38.p12 chr9: 11,854,684-12,151,781 , GRCh37.p13 chr9: 11,854,684-12,151,781 LOC105375976
    nsv4680750copy number variation1nstd189human GRCh38.p12 chr9: 11,919,134-12,210,618 , GRCh37.p13 chr9: 11,919,134-12,210,618 LOC105375976
    nsv4680749copy number variation1nstd189human GRCh38.p12 chr8: 128,970,130-129,261,043 , GRCh37.p13 chr8: 129,982,376-130,273,289 LINC00977
    nsv4679267copy number variation1nstd189human GRCh38.p12 chr10: 55,160,059-55,450,482 , GRCh37.p13 chr10: 56,919,819-57,210,242 PCDH15
    nsv4680455copy number variation1nstd189human GRCh38.p12 chr6: 161,726,240-162,011,300 , GRCh37.p13 chr6: 162,147,272-162,432,332 PRKN
    nsv4679281copy number variation1nstd189human GRCh38.p12 chr9: 11,645,593-11,929,890 , GRCh37.p13 chr9: 11,645,593-11,929,890 LOC101929446
    nsv4679636copy number variation1nstd189human GRCh38.p12 chr9: 11,905,557-12,182,949 , GRCh37.p13 chr9: 11,905,557-12,182,949 LOC105375976
    nsv4680792copy number variation1nstd189human GRCh38.p12 chr9: 11,645,593-11,922,842 , GRCh37.p13 chr9: 11,645,593-11,922,842 LOC101929446
    nsv4680986copy number variation1nstd189human GRCh38.p12 chr2: 35,589,011-35,865,335 , GRCh37.p13 chr2: 35,814,077-36,090,401 MRPL50P1
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