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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5557473sequence alteration1nstd206human GRCh38 chr1: 10,919,048-11,710,696 , GRCh37.p13 chr1: 10,979,105-11,770,753 , ANGPTL7, 26 more genes
    nsv4782959copy number variation1nstd200human GRCh37 chr1: 11,113,085-11,113,458 , GRCh38.p12 chr1: 11,053,028-11,053,401 SRM
    nsv4684113copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 11,053,101-11,336,968 , GRCh38.p12 chr1: 10,993,044-11,276,911 MTOR, EXOSC10, 11 more genes
    nsv4681090copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,072,691-11,994,922 , GRCh38.p12 chr1: 11,012,634-11,934,865 FBXO44, LINC01647, 36 more genes
    nsv4674729copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,908,411-11,158,092 , GRCh38.p12 chr1: 10,848,354-11,098,035 CFL1P6, SRM, 7 more genes
    nsv4674113copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,086,990-11,429,365 , GRCh38.p12 chr1: 11,026,933-11,369,308 RNU6-537P, UBE2V2P3, 13 more genes
    nsv4674003copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 9,852,396-11,909,475 , GRCh38.p12 chr1: 9,792,338-11,849,418 CLCN6, CORT, 59 more genes
    nsv4579013copy number variation1nstd183human GRCh37 chr1: 11,065,971-11,433,766 , GRCh38.p12 chr1: 11,005,914-11,373,709 RPL39P6, LOC105376739, 14 more genes
    nsv4454705copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,246,640-12,841,900 , GRCh38.p12 chr1: 10,186,582-12,781,757 LINC01647, MIR7846, 73 more genes
    nsv4436680complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-24,379,779 , GRCh37 chr1: 909,238-24,706,269 ALPL, RERE, 636 more genes
    nsv4436526complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-16,409,637 , GRCh37 chr1: 909,238-16,736,132 RERE, CA6, 415 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4436105copy number variation1nstd102humanPathogenic GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061 PARK7, RNF223, 325 more genes
    nsv4371624copy number variation1nstd173human GRCh37 chr1: 11,085,558-11,143,298 , GRCh38.p12 chr1: 11,025,501-11,083,241 TARDBP, SRM, 2 more genes
    nsv3913790copy number variation1nstd102humanPathogenic NCBI36 chr1: 10,370,726-15,979,918 , GRCh37.p13 chr1: 10,448,139-16,107,331 , GRCh38.p12 chr1: 10,388,082-15,780,836 PRAMEF15, LOC105376759, 149 more genes
    nsv3912305copy number variation1nstd102humanPathogenic NCBI36 chr1: 8,912,677-16,390,632 , GRCh37.p13 chr1: 8,990,090-16,518,045 , GRCh38.p12 chr1: 8,930,031-16,191,550 DDI2, RN7SL614P, 200 more genes
    nsv3908546copy number variation1nstd102humanPathogenic GRCh38 chr1: 6,554,885-16,056,011 , GRCh37 chr1: 6,614,945-16,382,506 , NCBI36 chr1: 6,537,532-16,255,093 LOC105376717, LOC107984915, 244 more genes
    nsv3905483copy number variation1nstd102humanPathogenic GRCh38 chr1: 6,303,641-15,799,093 , NCBI36 chr1: 6,286,288-15,998,175 , GRCh37 chr1: 6,363,701-16,125,588 VPS13D, PRAMEF30P, 240 more genes
    nsv3903672copy number variation1nstd102humanPathogenic GRCh38 chr1: 9,064,492-12,666,744 , NCBI36 chr1: 9,047,138-12,649,342 , GRCh37 chr1: 9,124,551-12,726,755 LOC105376712, CENPS, 101 more genes
    nsv3903444copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,958,499-13,178,528 , NCBI36 chr1: 4,858,359-13,101,115 , GRCh38 chr1: 4,898,439-13,111,056 NPPA-AS1, PARK7, 195 more genes
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