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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072420inversion1nstd229human GRCh38 chr14: 97,972,870-97,978,714 , GRCh37.p13 chr14: 98,439,207-98,445,051 LINC01550
    nsv7069900inversion1nstd229human GRCh38 chr14: 97,971,930-97,976,794 , GRCh37.p13 chr14: 98,438,267-98,443,131 LINC01550
    nsv6977948copy number variation1nstd229human GRCh38 chr14: 97,948,301-97,952,100 , GRCh37.p13 chr14: 98,414,638-98,418,437 LINC01550
    nsv6977854copy number variation1nstd229human GRCh38 chr14: 97,960,428-97,970,880 , GRCh37.p13 chr14: 98,426,765-98,437,217 LINC01550
    nsv6977848copy number variation1nstd229human GRCh38 chr14: 97,665,439-98,051,356 , GRCh37.p13 chr14: 98,131,776-98,517,693 LOC105370650, LINC01550, 4 more genes
    nsv6975741copy number variation1nstd229human GRCh38 chr14: 97,935,705-97,935,849 , GRCh37.p13 chr14: 98,402,042-98,402,186 LINC01550
    nsv6965255copy number variation1nstd229human GRCh38 chr14: 97,931,405-97,956,857 , GRCh37.p13 chr14: 98,397,742-98,423,194 LINC01550
    nsv6962844copy number variation1nstd229human GRCh38 chr14: 97,929,848-97,935,070 , GRCh37.p13 chr14: 98,396,185-98,401,407 LINC01550
    nsv6960772copy number variation1nstd229human GRCh38 chr14: 97,917,356-97,925,920 , GRCh37.p13 chr14: 98,383,693-98,392,257 LINC01550
    nsv6959376copy number variation1nstd229human GRCh38 chr14: 97,955,890-97,969,981 , GRCh37.p13 chr14: 98,422,227-98,436,318 LINC01550
    nsv6958828copy number variation1nstd229human GRCh38 chr14: 97,931,986-97,945,866 , GRCh37.p13 chr14: 98,398,323-98,412,203 LINC01550
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6505253copy number variation1nstd223human GRCh38 chr14: 97,937,611-97,938,227 , GRCh37.p13 chr14: 98,403,948-98,404,564 LINC01550
    nsv6501978copy number variation1nstd223human GRCh38 chr14: 97,929,840-97,935,069 , GRCh37.p13 chr14: 98,396,177-98,401,406 LINC01550
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6314295complex chromosomal rearrangement2nstd102humanUncertain significance GRCh38.p12 chr14: 97,944,614-97,944,614 , GRCh38.p12 chr14: 97,944,634-97,944,634 , GRCh37 chr14: 98,410,951-98,410,951 , GRCh37 chr14: 98,410,971-98,410,971 , GRCh38.p12 chr1: 60,538,572-60,538,572 , GRCh38.p12 chr1: 60,538,584-60,538,584 , GRCh37 chr1: 61,004,244-61,004,244 , GRCh37 chr1: 61,004,256-61,004,256 LINC01550, LINC01748
    nsv6291768copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186 CCDC85C, MEG3, 206 more genes
    nsv6274728copy number variation1nstd214human GRCh38 chr14: 97,953,676-97,953,735 , GRCh37.p13 chr14: 98,420,013-98,420,072 LINC01550
    nsv6241728mobile element insertion1nstd215human GRCh38 chr14: 97,953,659-97,953,659 , GRCh37.p13 chr14: 98,419,996-98,419,996 LINC01550
    nsv6241726mobile element insertion1nstd215human GRCh38 chr14: 97,940,304-97,940,304 , GRCh37.p13 chr14: 98,406,641-98,406,641 LINC01550
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