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Items: 1 to 20 of 56

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4457579copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,389,413-47,419,990 , GRCh38.p12 chr18: 49,863,043-49,893,620 MYO5B
    nsv7095383copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,398,517-47,405,480 , GRCh38.p12 chr18: 49,872,147-49,879,110 MYO5B
    nsv7095015copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 47,378,320-47,379,822 , GRCh38.p12 chr18: 49,851,950-49,853,452 MYO5B
    nsv7095016copy number variation1nstd102humanLikely pathogenic GRCh37 chr18: 47,479,610-47,480,825 , GRCh38.p12 chr18: 49,953,240-49,954,455 MYO5B
    nsv3906428copy number variation1nstd102humanBenign GRCh37 chr18: 47,695,103-47,698,268 , GRCh38.p12 chr18: 50,168,733-50,171,898 MYO5B
    nsv6310263copy number variation1nstd102humanUncertain significance GRCh37 chr18: 47,428,944-47,433,020 , GRCh38.p12 chr18: 49,902,574-49,906,650 MYO5B
    nsv4457528copy number variation1nstd102humanUncertain significance GRCh37 chr18: 47,573,928-47,610,802 , GRCh38.p12 chr18: 50,047,558-50,084,432 MYO5B, ADAD1P2
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 MYO5B, LOC107985176, 632 more genes
    nsv3902831copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,177,798-78,014,123 , GRCh38.p12 chr18: 48,651,427-80,256,240 MYO5B, LOC105372180, 370 more genes
    nsv3906152copy number variation1nstd102humanPathogenic GRCh37 chr18: 46,942,427-78,014,123 , GRCh38.p12 chr18: 49,416,057-80,256,240 MYO5B, RPL17P44, 360 more genes
    nsv3909519copy number variation1nstd102humanPathogenic GRCh37 chr18: 47,656,799-78,014,123 , GRCh38.p12 chr18: 50,130,429-80,256,240 MYO5B, LOC105372160, 339 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 MYO5B, LOC105372145, 947 more genes
    nsv3907444copy number variation1nstd102humanPathogenic GRCh37 chr18: 12,842-78,015,180 , GRCh38.p12 chr18: 12,842-80,257,297 MYO5B, GALNT1, 947 more genes
    nsv3890669copy number variation1nstd102humanPathogenic GRCh37 chr18: 13,034-78,015,180 , GRCh38.p12 chr18: 13,034-80,257,297 MYO5B, MYL12B, 947 more genes
    nsv3918488copy number variation1nstd102humanPathogenic NCBI36 chr18: 43,345-76,068,860 , GRCh38 chr18: 53,345-80,209,986 , GRCh37 chr18: 53,345-77,967,869 MYO5B, LOC105372027, 945 more genes
    nsv3924351copy number variation1nstd102humanPathogenic NCBI36 chr18: 108,760-76,113,817 , GRCh38 chr18: 118,760-80,254,946 , GRCh37 chr18: 118,760-78,012,829 MYO5B, MIX23P1, 942 more genes
    nsv3919004copy number variation1nstd102humanPathogenic GRCh38 chr18: 136,226-80,256,240 , GRCh37 chr18: 136,226-78,014,123 , NCBI36 chr18: 126,226-76,115,097 MYO5B, LIVAR, 941 more genes
    nsv3899451copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,226-78,014,123 , GRCh38.p12 chr18: 136,226-80,256,240 MYO5B, BOLA2P1, 941 more genes
    nsv3924706copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38 chr18: 136,227-80,256,240 , NCBI36 chr18: 126,227-76,115,097 MYO5B, LOC100420948, 941 more genes
    nsv3907722copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-78,014,123 , GRCh38.p12 chr18: 136,227-80,256,240 MYO5B, ROCK1, 941 more genes
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