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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148229copy number variation1nstd102humanPathogenic GRCh38 chr4: 2,904,667-42,963,232 , GRCh37.p13 chr4: 2,906,394-42,965,249 LINC01587, RN7SKP82, 509 more genes
    nsv7148161copy number variation1nstd102humanPathogenic GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194 SLIRPP2, STIM2-AS1, 659 more genes
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv7098857copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,245,868-39,700,010 , GRCh38.p12 chr4: 39,244,248-39,698,390 UGDH, UBE2K, 13 more genes
    nsv7097249copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,187,326-39,478,735 , GRCh38.p12 chr4: 39,185,706-39,477,115 RNU6-32P, RNU6-887P, 6 more genes
    nsv7096851copy number variation1nstd102humanUncertain significance GRCh37 chr4: 39,460,510-39,460,802 , GRCh38.p12 chr4: 39,458,890-39,459,182 RPL9, LIAS
    nsv7096849copy number variation1nstd102humanUncertain significance GRCh37 chr4: 38,765,721-39,478,735 , GRCh38.p12 chr4: 38,764,100-39,477,115 TMEM156, TLR6, 14 more genes
    nsv7049186inversion1nstd229human GRCh38 chr4: 38,135,041-40,245,309 , GRCh37.p13 chr4: 38,136,662-40,246,929 SMIM14, RNU6-887P, 42 more genes
    nsv7038584inversion1nstd229human GRCh38 chr4: 38,474,718-40,416,508 , GRCh37.p13 chr4: 38,476,339-40,418,525 RPL9, UBE2K, 41 more genes
    nsv6732875copy number variation1nstd229human GRCh38 chr4: 39,468,299-39,486,785 , GRCh37.p13 chr4: 39,469,919-39,488,405 LIAS, LOC401127
    nsv6728890copy number variation1nstd229human GRCh38 chr4: 39,473,901-39,538,500 , GRCh37.p13 chr4: 39,475,521-39,540,120 UGDH, LIAS, 2 more genes
    nsv6727182copy number variation1nstd229human GRCh38 chr4: 39,468,301-39,538,300 , GRCh37.p13 chr4: 39,469,921-39,539,920 LOC401127, UGDH-AS1, 2 more genes
    nsv6725831copy number variation1nstd229human GRCh38 chr4: 39,364,760-39,637,191 , GRCh37.p13 chr4: 39,366,380-39,638,811 SMIM14, RNU6-887P, 10 more genes
    nsv6724925copy number variation1nstd229human GRCh38 chr4: 39,423,604-39,530,372 , GRCh37.p13 chr4: 39,425,224-39,531,992 UGDH, RPL9, 4 more genes
    nsv6719466copy number variation1nstd229human GRCh38 chr4: 39,478,306-39,480,159 , GRCh37.p13 chr4: 39,479,926-39,481,779 LOC401127, LIAS
    nsv6634358copy number variation1nstd102humanPathogenic GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344 LINC02475, LOC105374344, 658 more genes
    nsv6629864copy number variation1nstd224human GRCh37 chr4: 39,247,063-39,548,112 , GRCh38.p12 chr4: 39,245,443-39,546,492 RFC1, UGDH, 10 more genes
    nsv6629487copy number variation1nstd224human GRCh37 chr4: 39,430,969-39,566,499 , GRCh38.p12 chr4: 39,429,349-39,564,879 RPL9, UGDH, 5 more genes
    nsv6629485copy number variation1nstd224human GRCh37 chr4: 39,358,598-39,518,110 , GRCh38.p12 chr4: 39,356,978-39,516,490 RFC1, RPL9, 6 more genes
    nsv6629442copy number variation1nstd224human GRCh37 chr4: 39,430,969-39,570,502 , GRCh38.p12 chr4: 39,429,349-39,568,882 RPL9, UGDH, 5 more genes
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