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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055819inversion1nstd229human GRCh37.p13 chr7|NW_003571037.1: 152,792-312,266 , GRCh38 chr7: 102,228,462-102,387,936 , GRCh37.p13 chr7: 101,871,742-102,028,383 LOC100289561, SH2B2, 6 more genes
    nsv7055390inversion1nstd229human GRCh38 chr7: 100,184,977-102,400,588 , GRCh37.p13 chr7: 99,782,600-101,718,950 SLC12A9-AS1, STAG3, 84 more genes
    nsv7040420inversion1nstd229human GRCh38 chr7: 101,445,712-104,173,878 , GRCh37.p13 chr7: 101,088,993-103,814,326 ALKBH4, RPS29P16, 54 more genes
    nsv6820207copy number variation1nstd229human GRCh38 chr7: 102,149,801-102,307,200 , GRCh37.p13 chr7: 101,793,081-101,950,483 , GRCh37.p13 chr7|NW_003571037.1: 74,131-231,530 SH2B2, MIR4285, 1 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631293copy number variation1nstd224human GRCh37 chr7: 101,870,948-102,113,373 , GRCh38.p12 chr7: 102,227,668-102,472,926 CUX1, ALKBH4, 15 more genes
    nsv6602521copy number variation1nstd223human GRCh38 chr7: 102,167,380-103,063,308 , GRCh37.p13 chr7: 102,072,448-102,703,755 MIR4467, MIR548O, 32 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
    nsv6291301copy number variation1nstd102humanUncertain significance GRCh37 chr7: 101,729,998-102,114,340 , GRCh38.p12 chr7: 102,086,718-102,473,893 LOC105375433, CUX1, 15 more genes
    nsv6136532copy number variation1nstd213human GRCh37 chr7: 101,870,000-102,140,001 , GRCh38.p12 chr7: 102,226,720-102,499,554 LRWD1, LOC100289561, 16 more genes
    nsv6136217copy number variation1nstd213human GRCh37 chr7: 99,390,000-104,070,001 , GRCh38.p12 chr7: 99,792,377-104,429,553 AZGP1, CRYZP1, 157 more genes
    nsv6107847inversion1nstd212human GRCh38 chr7: 100,184,978-102,378,892 , GRCh37.p13 chr7: 99,782,601-101,718,950 , ACHE, 87 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825220copy number variation1nstd200human GRCh37 chr7: 101,927,468-101,953,454 , GRCh38.p12 chr7: 102,284,176-102,310,172 MIR4285, CUX1, 1 more genes
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