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Items: 1 to 20 of 185

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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
    nsv6753763copy number variation1nstd229human GRCh38 chr4: 73,474,873-73,485,250 , GRCh37.p13 chr4: 74,340,590-74,350,967 AFM
    nsv6749672copy number variation1nstd229human GRCh38 chr4: 73,439,401-73,491,100 , GRCh37.p13 chr4: 74,305,118-74,356,817 AFM, AFP
    nsv6749452copy number variation1nstd229human GRCh38 chr4: 73,492,466-73,500,118 , GRCh37.p13 chr4: 74,358,183-74,365,835 AFM
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6747776copy number variation1nstd229human GRCh38 chr4: 73,500,749-73,501,325 , GRCh37.p13 chr4: 74,366,466-74,367,042 AFM
    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
    nsv6740073copy number variation1nstd229human GRCh38 chr4: 73,480,052-73,480,679 , GRCh37.p13 chr4: 74,345,769-74,346,396 AFM
    nsv6738521copy number variation1nstd229human GRCh38 chr4: 73,503,995-73,504,200 , GRCh37.p13 chr4: 74,369,712-74,369,917 AFM
    nsv6573599inversion1nstd223human GRCh38 chr4: 73,480,122-73,480,664 , GRCh37.p13 chr4: 74,345,839-74,346,381 AFM
    nsv6557569inversion1nstd223human GRCh38 chr4: 70,947,674-74,191,820 , GRCh37.p13 chr4: 71,813,391-75,057,537 , HNRNPA1P67, 44 more genes
    nsv6389712copy number variation1nstd223human GRCh38 chr4: 73,486,657-73,487,214 , GRCh37.p13 chr4: 74,352,374-74,352,931 AFM
    nsv6388655copy number variation1nstd223human GRCh38 chr4: 73,494,055-73,994,884 , GRCh37.p13 chr4: 74,359,772-74,860,601 , RASSF6, 13 more genes
    nsv6378672copy number variation1nstd223human GRCh38 chr4: 73,492,466-73,500,112 , GRCh37.p13 chr4: 74,358,183-74,365,829 AFM
    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
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