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Items: 1 to 20 of 299

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049375inversion1nstd229human GRCh38 chr3: 45,009,134-45,392,115 , GRCh37.p13 chr3: 45,050,626-45,433,607 LOC105377061, LOC101928636, 8 more genes
    nsv7043298inversion1nstd229human GRCh38 chr3: 45,112,656-45,115,752 , GRCh37.p13 chr3: 45,154,148-45,157,244 CDCP1
    nsv7040719inversion1nstd229human GRCh38 chr3: 45,127,693-45,127,798 , GRCh37.p13 chr3: 45,169,185-45,169,290 CDCP1
    nsv7038909inversion1nstd229human GRCh38 chr3: 40,520,096-45,093,302 , GRCh37.p13 chr3: 40,561,587-45,134,794 ABHD5, ZKSCAN7, 97 more genes
    nsv6717974copy number variation1nstd229human GRCh38 chr3: 45,026,284-45,219,335 , GRCh37.p13 chr3: 45,067,776-45,260,827 LOC101928636, CDCP1, 3 more genes
    nsv6710706copy number variation1nstd229human GRCh38 chr3: 44,976,101-45,108,500 , GRCh37.p13 chr3: 45,017,593-45,149,992 CLEC3B, EXOSC7, 3 more genes
    nsv6708579copy number variation1nstd229human GRCh38 chr3: 45,139,123-45,143,531 , GRCh37.p13 chr3: 45,180,615-45,185,023 CDCP1
    nsv6707483copy number variation1nstd229human GRCh38 chr3: 45,134,572-45,139,874 , GRCh37.p13 chr3: 45,176,064-45,181,366 CDCP1
    nsv6705288copy number variation1nstd229human GRCh38 chr3: 45,128,682-45,131,227 , GRCh37.p13 chr3: 45,170,174-45,172,719 CDCP1
    nsv6701957copy number variation1nstd229human GRCh38 chr3: 45,145,516-45,150,950 , GRCh37.p13 chr3: 45,187,008-45,192,442 CDCP1
    nsv6700792copy number variation1nstd229human GRCh38 chr3: 45,142,210-45,147,759 , GRCh37.p13 chr3: 45,183,702-45,189,251 CDCP1
    nsv6700154copy number variation1nstd229human GRCh38 chr3: 45,097,701-45,168,300 , GRCh37.p13 chr3: 45,139,193-45,209,792 CDCP1, RPS24P8
    nsv6629040copy number variation1nstd224human GRCh37 chr3: 45,077,252-45,162,682 , GRCh38.p12 chr3: 45,035,760-45,121,190 CDCP1, CLEC3B
    nsv6543270inversion1nstd223human GRCh38 chr3: 45,101,683-45,102,184 , GRCh37.p13 chr3: 45,143,175-45,143,676 CDCP1
    nsv6542675inversion1nstd223human GRCh38 chr3: 45,107,280-45,108,067 , GRCh37.p13 chr3: 45,148,772-45,149,559 CDCP1
    nsv6372673copy number variation1nstd223human GRCh38 chr3: 45,087,921-45,088,319 , GRCh37.p13 chr3: 45,129,413-45,129,811 CDCP1
    nsv6369016copy number variation1nstd223human GRCh38 chr3: 45,117,961-45,118,866 , GRCh37.p13 chr3: 45,159,453-45,160,358 CDCP1
    nsv6368904copy number variation1nstd223human GRCh38 chr3: 45,107,334-45,108,437 , GRCh37.p13 chr3: 45,148,826-45,149,929 CDCP1
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv6263468copy number variation1nstd214human GRCh38 chr3: 45,108,810-45,108,944 , GRCh37.p13 chr3: 45,150,302-45,150,436 CDCP1
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