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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044412inversion1nstd229human GRCh38 chr1: 27,748,482-27,751,146 , GRCh37.p13 chr1: 28,074,993-28,077,657 FAM76A
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648258copy number variation1nstd229human GRCh38 chr1: 27,439,701-27,781,300 , GRCh37.p13 chr1: 27,766,215-28,107,811 CHMP1AP1, STX12, 11 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6555583inversion1nstd223human GRCh38 chr1: 27,723,882-27,724,263 , GRCh37.p13 chr1: 28,050,393-28,050,774 FAM76A
    nsv6554025inversion1nstd223human GRCh38 chr1: 27,736,946-27,737,724 , GRCh37.p13 chr1: 28,063,457-28,064,235 FAM76A
    nsv6548918inversion1nstd223human GRCh38 chr1: 27,723,183-27,724,233 , GRCh37.p13 chr1: 28,049,694-28,050,744 FAM76A
    nsv6547465inversion1nstd223human GRCh38 chr1: 27,751,113-27,751,217 , GRCh37.p13 chr1: 28,077,624-28,077,728 FAM76A
    nsv6544120inversion1nstd223human GRCh38 chr1: 27,728,514-27,728,896 , GRCh37.p13 chr1: 28,055,025-28,055,407 FAM76A
    nsv6535746inversion1nstd223human GRCh38 chr1: 27,756,376-27,756,777 , GRCh37.p13 chr1: 28,082,887-28,083,288 FAM76A
    nsv6333945copy number variation1nstd223human GRCh38 chr1: 27,707,901-27,737,620 , GRCh37.p13 chr1: 28,034,412-28,064,131 FAM76A
    nsv6333556copy number variation1nstd223human GRCh38 chr1: 24,890,501-27,921,300 , GRCh37.p13 chr1: 25,216,992-28,247,811 RUNX3, MACO1, 108 more genes
    nsv6325626copy number variation1nstd223human GRCh38 chr1: 27,724,617-27,732,101 , GRCh37.p13 chr1: 28,051,128-28,058,612 FAM76A
    nsv6320655copy number variation1nstd223human GRCh38 chr1: 27,725,001-27,726,600 , GRCh37.p13 chr1: 28,051,512-28,053,111 FAM76A
    nsv6319313copy number variation1nstd223human GRCh38 chr1: 27,730,322-27,731,441 , GRCh37.p13 chr1: 28,056,833-28,057,952 FAM76A
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6258593mobile element insertion1nstd215human GRCh38 chr1: 27,734,873-27,734,873 , GRCh37.p13 chr1: 28,061,384-28,061,384 FAM76A
    nsv6133648copy number variation1nstd213human GRCh37 chr1: 23,300,000-28,930,001 , GRCh38.p12 chr1: 22,973,507-28,603,489 RUNX3, CD52, 195 more genes
    nsv5883926copy number variation1nstd209human GRCh38 chr1: 27,748,333-27,748,534 , GRCh37.p13 chr1: 28,074,844-28,075,045 FAM76A
    nsv5829674copy number variation2nstd209human GRCh38 chr1: 27,758,905-27,760,004 , GRCh37.p13 chr1: 28,085,416-28,086,515 FAM76A
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