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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052940inversion1nstd229human GRCh38 chr4: 73,455,263-76,320,440 , GRCh37.p13 chr4: 74,320,980-77,241,593 , RASSF6, 65 more genes
    nsv7051444inversion1nstd229human GRCh38 chr4: 70,947,675-74,191,821 , GRCh37.p13 chr4: 71,813,392-75,057,538 , COX18, 44 more genes
    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
    nsv6752969copy number variation1nstd229human GRCh38 chr4: 73,583,066-74,060,724 , GRCh37.p13 chr4: 74,448,783-74,926,441 , CXCL6, 14 more genes
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6740221copy number variation1nstd229human GRCh38 chr4: 71,124,425-74,382,728 , GRCh37.p13 chr4: 71,990,142-75,248,445 , ALB, 45 more genes
    nsv6558067inversion1nstd223human GRCh38 chr4: 73,733,714-73,754,584 , GRCh37.p13 chr4: 74,599,431-74,620,301 CXCL8
    nsv6557569inversion1nstd223human GRCh38 chr4: 70,947,674-74,191,820 , GRCh37.p13 chr4: 71,813,391-75,057,537 , HNRNPA1P67, 44 more genes
    nsv6388655copy number variation1nstd223human GRCh38 chr4: 73,494,055-73,994,884 , GRCh37.p13 chr4: 74,359,772-74,860,601 , RASSF6, 13 more genes
    nsv6382898copy number variation1nstd223human GRCh38 chr4: 73,740,833-73,747,038 , GRCh37.p13 chr4: 74,606,550-74,612,755 CXCL8
    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
    nsv6313740copy number variation1nstd102humanPathogenic GRCh37 chr4: 61,867,555-74,711,517 , GRCh38.p12 chr4: 61,001,837-73,845,800 CXCL8, UGT2A1, 175 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
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6135084copy number variation1nstd213human GRCh37 chr4: 74,050,000-74,670,001 , GRCh38.p12 chr4: 73,184,283-73,804,284 , AFM, 8 more genes
    nsv6134946copy number variation1nstd213human GRCh37 chr4: 73,030,000-74,850,001 , GRCh38.p12 chr4: 72,164,283-73,984,284 , AFP, 24 more genes
    nsv5976857inversion1nstd209human GRCh38 chr4: 73,733,711-73,754,583 , GRCh37.p13 chr4: 74,599,428-74,620,300 CXCL8
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5840377copy number variation1nstd209human GRCh38 chr4: 73,733,680-73,739,328 , GRCh37.p13 chr4: 74,599,397-74,605,045 CXCL8
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