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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7097256copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr4: 55,124,936-57,368,027 , GRCh38.p12 chr4: 54,258,769-56,501,861 AASDH, EXOC1, 40 more genes
    nsv7057463inversion1nstd229human GRCh38 chr4: 55,971,062-55,971,099 , GRCh37.p13 chr4: 56,837,228-56,837,265 CEP135
    nsv7042838inversion1nstd229human GRCh38 chr4: 55,519,343-61,509,140 , GRCh37.p13 chr4: 56,385,510-62,374,858 LINC02271, CHAER1, 59 more genes
    nsv6737683copy number variation1nstd229human GRCh38 chr4: 56,001,526-56,010,359 , GRCh37.p13 chr4: 56,867,692-56,876,525 CEP135
    nsv6737087copy number variation1nstd229human GRCh38 chr4: 55,978,817-55,981,844 , GRCh37.p13 chr4: 56,844,983-56,848,010 CEP135
    nsv6736079copy number variation1nstd229human GRCh38 chr4: 55,999,857-56,012,406 , GRCh37.p13 chr4: 56,866,023-56,878,572 CEP135
    nsv6732261copy number variation1nstd229human GRCh38 chr4: 55,692,600-55,954,831 , GRCh37.p13 chr4: 56,558,767-56,820,997 EXOC1, RNU6-276P, 5 more genes
    nsv6732141copy number variation1nstd229human GRCh38 chr4: 56,013,631-56,019,965 , GRCh37.p13 chr4: 56,879,797-56,886,131 CEP135
    nsv6731112copy number variation1nstd229human GRCh38 chr4: 55,973,608-55,973,846 , GRCh37.p13 chr4: 56,839,774-56,840,012 CEP135
    nsv6730838copy number variation1nstd229human GRCh38 chr4: 55,861,538-56,010,693 , GRCh37.p13 chr4: 56,727,704-56,876,859 CEP135, EXOC1, 2 more genes
    nsv6729650copy number variation1nstd229human GRCh38 chr4: 56,032,001-57,014,500 , GRCh37.p13 chr4: 56,898,167-57,880,666 REST, RPL7AP31, 27 more genes
    nsv6728489copy number variation1nstd229human GRCh38 chr4: 56,000,813-56,003,709 , GRCh37.p13 chr4: 56,866,979-56,869,875 CEP135
    nsv6727577copy number variation1nstd229human GRCh38 chr4: 56,008,275-56,391,694 , GRCh37.p13 chr4: 56,874,441-57,257,860 RNA5SP162, RNU6-197P, 8 more genes
    nsv6727179copy number variation1nstd229human GRCh38 chr4: 55,964,370-55,966,230 , GRCh37.p13 chr4: 56,830,536-56,832,396 CEP135
    nsv6726590copy number variation1nstd229human GRCh38 chr4: 56,031,042-56,031,068 , GRCh37.p13 chr4: 56,897,208-56,897,234 CEP135
    nsv6725139copy number variation1nstd229human GRCh38 chr4: 55,960,925-55,961,792 , GRCh37.p13 chr4: 56,827,091-56,827,958 CEP135
    nsv6723185copy number variation1nstd229human GRCh38 chr4: 55,985,101-56,050,400 , GRCh37.p13 chr4: 56,851,267-56,916,566 CRACD, CEP135
    nsv6720692copy number variation1nstd229human GRCh38 chr4: 56,000,801-56,003,900 , GRCh37.p13 chr4: 56,866,967-56,870,066 CEP135
    nsv6720279copy number variation1nstd229human GRCh38 chr4: 55,564,862-55,964,774 , GRCh37.p13 chr4: 56,431,029-56,830,940 EXOC1, NMU, 8 more genes
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