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Items: 1 to 20 of 287

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv6937961copy number variation1nstd229human GRCh38 chr13: 27,549,188-27,552,744 , GRCh37.p13 chr13: 28,123,325-28,126,881 LNX2
    nsv6937745copy number variation1nstd229human GRCh38 chr13: 27,580,601-27,620,200 , GRCh37.p13 chr13: 28,154,738-28,194,337 POLR1D, LNX2
    nsv6935544copy number variation1nstd229human GRCh38 chr13: 27,570,756-27,570,784 , GRCh37.p13 chr13: 28,144,893-28,144,921 LNX2
    nsv6930563copy number variation1nstd229human GRCh38 chr13: 27,129,201-27,579,100 , GRCh37.p13 chr13: 27,703,338-28,153,237 MTIF3, USP12-AS1, 14 more genes
    nsv6930281copy number variation1nstd229human GRCh38 chr13: 27,619,239-27,619,279 , GRCh37.p13 chr13: 28,193,376-28,193,416 POLR1D, LNX2
    nsv6928577copy number variation1nstd229human GRCh38 chr13: 27,592,390-27,610,223 , GRCh37.p13 chr13: 28,166,527-28,184,360 LNX2
    nsv6928145copy number variation1nstd229human GRCh38 chr13: 27,559,344-27,559,377 , GRCh37.p13 chr13: 28,133,481-28,133,514 LNX2
    nsv6928085copy number variation1nstd229human GRCh38 chr13: 27,589,901-27,590,800 , GRCh37.p13 chr13: 28,164,038-28,164,937 LNX2
    nsv6923167copy number variation1nstd229human GRCh38 chr13: 27,590,799-27,591,383 , GRCh37.p13 chr13: 28,164,936-28,165,520 LNX2
    nsv6920474copy number variation1nstd229human GRCh38 chr13: 27,261,701-27,553,400 , GRCh37.p13 chr13: 27,835,838-28,127,537 RNY1P1, MTIF3, 6 more genes
    nsv6920166copy number variation1nstd229human GRCh38 chr13: 27,620,254-27,627,860 , GRCh37.p13 chr13: 28,194,391-28,201,997 LNX2, POLR1D
    nsv6918151copy number variation1nstd229human GRCh38 chr13: 27,165,601-27,598,600 , GRCh37.p13 chr13: 27,739,738-28,172,737 RASL11A, LOC105370126, 14 more genes
    nsv6637188copy number variation1nstd102humanUncertain significance GRCh37 chr13: 28,063,413-28,185,279 , GRCh38.p12 chr13: 27,489,276-27,611,142 LNX2
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6577908inversion1nstd223human GRCh38 chr13: 27,612,680-27,613,616 , GRCh37.p13 chr13: 28,186,817-28,187,753 LNX2
    nsv6484860copy number variation1nstd223human GRCh38 chr13: 27,583,246-27,593,734 , GRCh37.p13 chr13: 28,157,383-28,167,871 LNX2
    nsv6481146copy number variation1nstd223human GRCh38 chr13: 27,620,001-27,620,600 , GRCh37.p13 chr13: 28,194,138-28,194,737 POLR1D, LNX2
    nsv6476713copy number variation1nstd223human GRCh38 chr13: 27,558,101-27,559,400 , GRCh37.p13 chr13: 28,132,238-28,133,537 LNX2
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
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