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Items: 1 to 20 of 29

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3915021copy number variation1nstd102humanBenign NCBI36 chr3: 181,148,817-181,382,041 , GRCh37 chr3: 179,666,123-179,899,347 , GRCh38 chr3: 179,948,335-180,181,559 PEX5L, RNA5SP149
    nsv3913254copy number variation1nstd102humanPathogenic NCBI36 chr3: 175,313,014-183,652,825 , GRCh37.p13 chr3: 173,830,320-182,170,131 , GRCh38.p12 chr3: 174,112,530-182,452,343 PEX5L, RNU6-486P, 88 more genes
    nsv6634512copy number variation1nstd102humanPathogenic GRCh38 chr3: 179,547,548-182,152,788 , GRCh37.p13 chr3: 179,265,336-181,870,576 PEX5L, LOC105374243, 34 more genes
    nsv4728751copy number variation1nstd102humanPathogenic GRCh37 chr3: 179,016,729-181,527,320 , GRCh38.p12 chr3: 179,298,941-181,809,532 PEX5L, NDUFB5, 33 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 PEX5L, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 PEX5L, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 PEX5L, RPL23AP49, 2875 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 PEX5L, LINC02614, 1469 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 PEX5L, LOC105374179, 785 more genes
    nsv3874894copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426 PEX5L, RNU6-901P, 673 more genes
    nsv3918066copy number variation1nstd102humanPathogenic GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254 PEX5L, LOC105374260, 696 more genes
    nsv3918149copy number variation1nstd102humanPathogenic GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383 PEX5L, LINC02031, 647 more genes
    nsv3913128copy number variation1nstd102humanPathogenic GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323 PEX5L, SNORA4, 644 more genes
    nsv3914686copy number variation1nstd102humanPathogenic NCBI36 chr3: 158,493,861-199,345,995 , GRCh37 chr3: 157,011,167-197,861,598 , GRCh38 chr3: 157,293,378-198,134,727 PEX5L, RPL34P10, 625 more genes
    nsv3871065copy number variation1nstd102humanPathogenic GRCh37 chr3: 158,980,631-197,766,890 , GRCh38.p12 chr3: 159,262,842-198,040,019 PEX5L, LINC02048, 599 more genes
    nsv3912173copy number variation1nstd102humanPathogenic NCBI36 chr3: 167,337,691-199,336,383 , GRCh37 chr3: 165,854,997-197,851,986 , GRCh38 chr3: 166,137,209-198,125,115 PEX5L, LOC105374277, 540 more genes
    nsv3918982copy number variation1nstd102humanPathogenic GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178 PEX5L, EIF4G1, 515 more genes
    nsv3871599copy number variation1nstd102humanPathogenic GRCh37 chr3: 173,281,266-197,838,262 , GRCh38.p12 chr3: 173,563,476-198,111,391 PEX5L, LOC105374263, 436 more genes
    nsv3889215copy number variation1nstd102humanPathogenic GRCh37 chr3: 157,128,738-181,637,333 , GRCh38.p12 chr3: 157,410,949-181,919,545 PEX5L, NAALADL2, 274 more genes
    nsv3922385copy number variation1nstd102humanPathogenic NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383 PEX5L, LINC02053, 414 more genes
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