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Items: 1 to 20 of 171

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6757653copy number variation1nstd229human GRCh38 chr4: 73,357,652-73,412,208 , GRCh37.p13 chr4: 74,223,369-74,277,925 ALB, ANKRD17-DT
    nsv6752791copy number variation1nstd229human GRCh38 chr4: 73,417,665-73,476,892 , GRCh37.p13 chr4: 74,283,382-74,342,609 AFP, ALB
    nsv6750178copy number variation1nstd229human GRCh38 chr4: 73,399,901-73,404,100 , GRCh37.p13 chr4: 74,265,618-74,269,817 ALB
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6746769copy number variation1nstd229human GRCh38 chr4: 69,087,431-73,565,096 , GRCh37.p13 chr4: 69,953,149-74,430,813 LOC642496, CSN2, 76 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
    nsv6557569inversion1nstd223human GRCh38 chr4: 70,947,674-74,191,820 , GRCh37.p13 chr4: 71,813,391-75,057,537 , HNRNPA1P67, 44 more genes
    nsv6388055copy number variation1nstd223human GRCh38 chr4: 73,408,099-73,408,493 , GRCh37.p13 chr4: 74,273,816-74,274,210 ALB
    nsv6376850copy number variation1nstd223human GRCh38 chr4: 73,399,955-73,404,115 , GRCh37.p13 chr4: 74,265,672-74,269,832 ALB
    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
    nsv5894150copy number variation1nstd209human GRCh38 chr4: 73,399,955-73,404,114 , GRCh37.p13 chr4: 74,265,672-74,269,831 ALB
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
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