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Items: 1 to 20 of 493

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5671625inversion1nstd207human GRCh38 chr8: 7,301,025-12,600,730 , GRCh37.p13 chr8: 7,158,547-12,458,239 , BLK, 188 more genes
    nsv5627579insertion1nstd207human GRCh38 chr8: 12,184,052-12,184,052 , GRCh37.p13 chr8: 12,041,561-12,041,561 FAM86B1, FAM85A
    nsv5584231copy number variation1nstd207human GRCh38 chr8: 12,183,089-12,183,192 , GRCh37.p13 chr8: 12,040,598-12,040,701 ALG1L11P, FAM86B1
    nsv5258330copy number variation1nstd204human GRCh38.p13 chr8: 12,169,901-12,180,900 , GRCh37.p13 chr8: 12,027,410-12,038,409 FAM86B1, ALG1L11P, 1 more genes
    nsv5257663copy number variation1nstd204human GRCh38.p13 chr8: 12,188,201-12,191,700 , GRCh37.p13 chr8: 12,045,710-12,049,209 FAM85A, FAM86B1
    nsv5257642copy number variation1nstd204human GRCh38.p13 chr8: 12,177,701-12,180,400 , GRCh37.p13 chr8: 12,035,210-12,037,909 ALG1L11P, FAM90A2P, 1 more genes
    nsv5257418copy number variation1nstd204human GRCh38.p13 chr8: 12,188,201-12,218,500 , GRCh37.p13 chr8: 12,045,710-12,076,009 FAM86B1, ENPP7P12, 1 more genes
    nsv5256396copy number variation1nstd204human GRCh38.p13 chr8: 12,176,901-12,184,100 , GRCh37.p13 chr8: 12,034,410-12,041,609 ALG1L11P, FAM90A2P, 2 more genes
    nsv5256231copy number variation1nstd204human GRCh38.p13 chr8: 12,182,001-12,192,600 , GRCh37.p13 chr8: 12,039,510-12,050,109 FAM86B1, FAM85A, 1 more genes
    nsv5255399copy number variation1nstd204human GRCh38.p13 chr8: 12,173,501-12,226,800 , GRCh37.p13 chr8: 12,031,010-12,084,309 ALG1L11P, FAM90A2P, 3 more genes
    nsv5254218copy number variation1nstd204human GRCh38.p13 chr8: 12,175,801-12,195,800 , GRCh37.p13 chr8: 12,033,310-12,053,309 ALG1L11P, FAM90A2P, 2 more genes
    nsv5254168copy number variation1nstd204human GRCh38.p13 chr8: 12,180,701-12,186,300 , GRCh37.p13 chr8: 12,038,210-12,043,809 FAM85A, ALG1L11P, 1 more genes
    nsv5254035copy number variation1nstd204human GRCh38.p13 chr8: 12,184,101-12,188,300 , GRCh37.p13 chr8: 12,041,610-12,045,809 FAM85A, FAM86B1
    nsv5253820copy number variation1nstd204human GRCh38.p13 chr8: 12,183,801-12,192,700 , GRCh37.p13 chr8: 12,041,310-12,050,209 FAM86B1, FAM85A
    nsv5253551copy number variation1nstd204human GRCh38.p13 chr8: 12,173,501-12,195,400 , GRCh37.p13 chr8: 12,031,010-12,052,909 ALG1L11P, FAM90A2P, 2 more genes
    nsv5253467copy number variation1nstd204human GRCh38.p13 chr8: 12,190,001-12,194,800 , GRCh37.p13 chr8: 12,047,510-12,052,309 FAM85A, FAM86B1
    nsv5253361copy number variation1nstd204human GRCh38.p13 chr8: 12,179,001-12,180,300 , GRCh37.p13 chr8: 12,036,510-12,037,809 ALG1L11P, FAM86B1
    nsv5253353copy number variation1nstd204human GRCh37.p13 chr8: 12,008,610-12,052,109 , GRCh38.p13 chr8: 12,151,101-12,194,600 FAM86B1, DEFB109D, 4 more genes
    nsv5251300copy number variation1nstd204human GRCh37.p13 chr8: 11,997,210-12,084,309 , GRCh38.p13 chr8: 12,139,701-12,226,800 FAM86B1, DEFB109D, 5 more genes
    nsv5250663copy number variation1nstd204human GRCh38.p13 chr8: 12,173,501-12,229,600 , GRCh37.p13 chr8: 12,031,010-12,087,109 ENPP7P12, FAM85A, 3 more genes
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