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Items: 1 to 20 of 148

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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
    nsv6575549inversion1nstd223human GRCh38 chr4: 73,839,193-73,995,312 , GRCh37.p13 chr4: 74,704,910-74,861,029 CXCL1, PF4, 7 more genes
    nsv6557569inversion1nstd223human GRCh38 chr4: 70,947,674-74,191,820 , GRCh37.p13 chr4: 71,813,391-75,057,537 , HNRNPA1P67, 44 more genes
    nsv6391931copy number variation1nstd223human GRCh38 chr4: 73,832,201-73,841,000 , GRCh37.p13 chr4: 74,697,918-74,706,717 CXCL6
    nsv6388655copy number variation1nstd223human GRCh38 chr4: 73,494,055-73,994,884 , GRCh37.p13 chr4: 74,359,772-74,860,601 , RASSF6, 13 more genes
    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
    nsv6155340copy number variation1nstd214human GRCh38 chr4: 73,836,029-73,836,145 , GRCh37.p13 chr4: 74,701,746-74,701,862 CXCL6
    nsv6152688copy number variation1nstd214human GRCh38 chr4: 73,836,044-73,836,160 , GRCh37.p13 chr4: 74,701,761-74,701,877 CXCL6
    nsv6150991copy number variation1nstd214human GRCh38 chr4: 73,836,079-73,836,196 , GRCh37.p13 chr4: 74,701,796-74,701,913 CXCL6
    nsv6149665copy number variation1nstd214human GRCh38 chr4: 73,836,060-73,836,177 , GRCh37.p13 chr4: 74,701,777-74,701,894 CXCL6
    nsv6135085copy number variation1nstd213human GRCh37 chr4: 74,670,000-74,730,001 , GRCh38.p12 chr4: 73,804,283-73,864,284 PF4V1, CXCL6, 1 more genes
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