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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7092691copy number variation1nstd229human GRCh38 chrX: 90,583,822-99,472,797 , GRCh37.p13 chrX: 89,838,821-98,727,795 RNU2-26P, KRT18P11, 57 more genes
    nsv7082094copy number variation1nstd229human GRCh38 chrX: 97,896,485-97,985,334 , GRCh37.p13 chrX: 97,151,483-97,240,332 KPNB1P1, NCKAP1P1
    nsv7082092copy number variation1nstd229human GRCh38 chrX: 97,885,737-98,588,060 , GRCh37.p13 chrX: 97,140,735-97,843,058 LOC100420955, EEF1A1P15, 4 more genes
    nsv7082091copy number variation1nstd229human GRCh38 chrX: 97,884,300-97,956,118 , GRCh37.p13 chrX: 97,139,298-97,211,116 NCKAP1P1
    nsv7082088copy number variation1nstd229human GRCh38 chrX: 97,869,301-97,912,300 , GRCh37.p13 chrX: 97,124,299-97,167,298 NCKAP1P1
    nsv7082087copy number variation1nstd229human GRCh38 chrX: 97,869,301-97,907,700 , GRCh37.p13 chrX: 97,124,299-97,162,698 NCKAP1P1
    nsv7082086copy number variation1nstd229human GRCh38 chrX: 97,851,172-98,028,381 , GRCh37.p13 chrX: 97,106,170-97,283,379 NCKAP1P1, KPNB1P1
    nsv7082084copy number variation1nstd229human GRCh38 chrX: 97,832,901-97,978,000 , GRCh37.p13 chrX: 97,087,899-97,232,998 NCKAP1P1, ERVFC1, 1 more genes
    nsv7082068copy number variation1nstd229human GRCh38 chrX: 97,695,748-97,916,809 , GRCh37.p13 chrX: 96,950,747-97,171,807 NCKAP1P1, ERVFC1
    nsv7082053copy number variation1nstd229human GRCh38 chrX: 97,602,182-98,017,696 , GRCh37.p13 chrX: 96,857,181-97,272,694 NCKAP1P1, ERVFC1, 2 more genes
    nsv7082043copy number variation1nstd229human GRCh38 chrX: 97,529,447-98,017,697 , GRCh37.p13 chrX: 96,784,446-97,272,695 ERVFC1, DIAPH2, 3 more genes
    nsv7082029copy number variation1nstd229human GRCh38 chrX: 97,422,102-98,182,822 , GRCh37.p13 chrX: 96,677,101-97,437,820 ERVFC1, DIAPH2-AS1, 3 more genes
    nsv7082006copy number variation1nstd229human GRCh38 chrX: 97,283,366-97,916,002 , GRCh37.p13 chrX: 96,538,365-97,171,000 NCKAP1P1, DIAPH2, 3 more genes
    nsv7055859inversion1nstd229human GRCh38 chrX: 97,018,286-100,819,204 , GRCh37.p13 chrX: 96,273,285-100,074,193 RN7SL74P, PPIAP89, 21 more genes
    nsv7052177inversion1nstd229human GRCh38 chrX: 96,056,744-98,308,879 , GRCh37.p13 chrX: 95,311,743-97,563,877 RPS29P28, NDUFB5P2, 15 more genes
    nsv7050681inversion1nstd229human GRCh38 chrX: 97,861,259-97,976,003 , GRCh37.p13 chrX: 97,116,257-97,231,001 NCKAP1P1, KPNB1P1
    nsv7047882inversion1nstd229human GRCh38 chrX: 96,054,797-100,053,452 , GRCh37.p13 chrX: 95,309,796-99,308,450 RPL6P29, LOC101928508, 20 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 more genes
    nsv6634400copy number variation1nstd102humanPathogenic GRCh37 chrX: 90,868,186-99,828,437 , GRCh38.p12 chrX: 91,613,187-100,573,440 LOC100420872, LOC100420955, 55 more genes
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