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Items: 1 to 20 of 238

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142764insertion1nstd232human GRCh37.p13 chr4: 76,412,708-76,412,708 , GRCh38.p12 chr4: 75,487,498-75,487,498 RCHY1
    nsv7141401insertion1nstd232human GRCh37.p13 chr4: 76,407,874-76,407,874 , GRCh38.p12 chr4: 75,482,664-75,482,664 RCHY1
    nsv7052940inversion1nstd229human GRCh38 chr4: 73,455,263-76,320,440 , GRCh37.p13 chr4: 74,320,980-77,241,593 , RASSF6, 65 more genes
    nsv7049363inversion1nstd229human GRCh38 chr4: 75,500,736-75,506,942 , GRCh37.p13 chr4: 76,425,946-76,432,152 RCHY1
    nsv7045939inversion1nstd229human GRCh38 chr4: 69,867,306-75,844,103 , GRCh37.p13 chr4: 70,733,024-76,765,256 , PF4V1, 99 more genes
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv6750514copy number variation1nstd229human GRCh38 chr4: 75,494,133-75,494,530 , GRCh37.p13 chr4: 76,419,343-76,419,740 RCHY1
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6746687copy number variation1nstd229human GRCh38 chr4: 75,497,144-75,501,269 , GRCh37.p13 chr4: 76,422,354-76,426,479 RCHY1
    nsv6741882copy number variation1nstd229human GRCh38 chr4: 75,498,612-75,498,744 , GRCh37.p13 chr4: 76,423,822-76,423,954 RCHY1
    nsv6629734copy number variation1nstd224human GRCh37 chr4: 75,543,289-76,407,821 , GRCh38.p12 chr4: 74,618,075-75,482,611 BTC, LINC02483, 11 more genes
    nsv6565303inversion1nstd223human GRCh38 chr4: 75,501,246-75,502,021 , GRCh37.p13 chr4: 76,426,456-76,427,231 RCHY1
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
    nsv6388540copy number variation1nstd223human GRCh38 chr4: 75,487,801-75,489,900 , GRCh37.p13 chr4: 76,413,011-76,415,110 RCHY1
    nsv6381445copy number variation1nstd223human GRCh38 chr4: 75,506,944-75,507,389 , GRCh37.p13 chr4: 76,432,154-76,432,599 RCHY1
    nsv6381246copy number variation1nstd223human GRCh38 chr4: 75,497,144-75,501,270 , GRCh37.p13 chr4: 76,422,354-76,426,480 RCHY1
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv6313802copy number variation1nstd102humanUncertain significance GRCh37 chr4: 75,876,865-76,546,874 , GRCh38.p12 chr4: 74,951,655-75,621,690 THAP6, LOC107986230, 10 more genes
    nsv6313715copy number variation1nstd102humanPathogenic GRCh37 chr4: 73,055,313-80,083,154 , GRCh38.p12 chr4: 72,189,596-79,162,000 CCNG2, FTLP9, 129 more genes
    nsv6313510copy number variation1nstd102humanPathogenic GRCh37 chr4: 75,737,340-91,131,156 , GRCh38.p12 chr4: 74,812,130-90,210,005 HIGD1AP13, CXCL11, 240 more genes
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