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Items: 1 to 20 of 902

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7055285inversion1nstd229human GRCh38 chr4: 79,273,454-79,278,335 , GRCh37.p13 chr4: 80,194,608-80,199,489 LINC01088, NAA11
    nsv7054808inversion1nstd229human GRCh38 chr4: 79,272,013-79,278,668 , GRCh37.p13 chr4: 80,193,167-80,199,822 LINC01088, NAA11
    nsv7054149inversion1nstd229human GRCh38 chr4: 79,216,923-83,461,355 , GRCh37.p13 chr4: 80,138,077-84,382,508 RNU6-615P, ANTXR2, 63 more genes
    nsv7050594inversion1nstd229human GRCh38 chr4: 79,163,448-79,167,744 , GRCh37.p13 chr4: 80,084,602-80,088,898 LINC01088, NAA11
    nsv7049185inversion1nstd229human GRCh38 chr4: 77,808,799-83,184,403 , GRCh37.p13 chr4: 78,729,953-84,105,556 VAMP9P, HNRNPA3P13, 75 more genes
    nsv7048905inversion1nstd229human GRCh38 chr4: 79,161,853-79,175,149 , GRCh37.p13 chr4: 80,083,007-80,096,303 NAA11, LINC01088
    nsv7047380inversion1nstd229human GRCh38 chr4: 79,177,913-79,184,379 , GRCh37.p13 chr4: 80,099,067-80,105,533 NAA11, LINC01088
    nsv7041471inversion1nstd229human GRCh38 chr4: 79,074,391-79,076,091 , GRCh37.p13 chr4: 79,995,545-79,997,245 LINC01088
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv7038629inversion1nstd229human GRCh38 chr4: 79,160,840-79,160,944 , GRCh37.p13 chr4: 80,081,994-80,082,098 NAA11, LINC01088
    nsv7038602inversion1nstd229human GRCh38 chr4: 79,060,928-79,060,954 , GRCh37.p13 chr4: 79,982,082-79,982,108 LINC01088
    nsv6756328copy number variation1nstd229human GRCh38 chr4: 79,252,828-79,343,993 , GRCh37.p13 chr4: 80,173,982-80,265,147 NAA11, LINC01088
    nsv6756174copy number variation1nstd229human GRCh38 chr4: 79,100,887-79,124,525 , GRCh37.p13 chr4: 80,022,041-80,045,679 LINC01088
    nsv6755156copy number variation1nstd229human GRCh38 chr4: 79,289,822-79,590,896 , GRCh37.p13 chr4: 80,210,976-80,512,050 GK2, LINC01088, 5 more genes
    nsv6753665copy number variation1nstd229human GRCh38 chr4: 79,101,437-79,139,105 , GRCh37.p13 chr4: 80,022,591-80,060,259 LINC01088
    nsv6753368copy number variation1nstd229human GRCh38 chr4: 79,229,101-79,234,300 , GRCh37.p13 chr4: 80,150,255-80,155,454 LINC01088, NAA11
    nsv6752817copy number variation1nstd229human GRCh38 chr4: 79,236,816-79,273,249 , GRCh37.p13 chr4: 80,157,970-80,194,403 LINC01088, NAA11
    nsv6752400copy number variation1nstd229human GRCh38 chr4: 79,136,167-79,136,253 , GRCh37.p13 chr4: 80,057,321-80,057,407 LINC01088
    nsv6751894copy number variation1nstd229human GRCh38 chr4: 79,045,900-79,054,251 , GRCh37.p13 chr4: 79,967,054-79,975,405 LINC01088
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