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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097148copy number variation1nstd102humanPathogenic GRCh37 chr5: 52,285,299-56,189,507 , GRCh38.p12 chr5: 52,989,469-56,893,680 RPL37P25, CCNO, 69 more genes
    nsv7057901inversion1nstd229human GRCh38 chr5: 53,201,194-56,162,991 , GRCh37.p13 chr5: 52,497,024-55,458,818 , PLPP1, 55 more genes
    nsv7056130inversion1nstd229human GRCh38 chr5: 53,218,622-56,162,980 , GRCh37.p13 chr5: 52,514,452-55,458,807 , ASS1P9, 54 more genes
    nsv6766352copy number variation1nstd229human GRCh38 chr5: 52,086,933-59,394,572 , GRCh37.p13 chr5: 51,382,767-58,690,398 , LOC105378980, 102 more genes
    nsv6412724copy number variation1nstd223human GRCh38 chr5: 55,167,201-55,178,300 , GRCh37.p13 chr5: 54,463,029-54,474,128 CDC20B, GPX8, 3 more genes
    nsv6407236copy number variation1nstd223human GRCh38 chr5: 55,161,701-55,260,700 , GRCh37.p13 chr5: 54,457,529-54,556,528 CCNO, DHX29, 6 more genes
    nsv6135669copy number variation1nstd213human GRCh37 chr5: 49,470,000-58,470,001 , GRCh38.p12 chr5: 50,174,166-59,174,175 , ASS1P9, 120 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv5094141mobile element insertion1nstd203human GRCh38 chr5: 55,166,675-55,166,689 , GRCh37.p13 chr5: 54,462,503-54,462,517 CDC20B, GPX8
    nsv4451131copy number variation1nstd102humanUncertain significance GRCh37 chr5: 53,180,658-54,552,379 , GRCh38.p12 chr5: 53,884,828-55,256,551 HSPB3, LOC102467081, 25 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
    nsv3923429copy number variation1nstd102humanPathogenic GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770 ISCA1P1, LOC643307, 163 more genes
    nsv3922909copy number variation1nstd102humanPathogenic GRCh38 chr5: 50,462,100-55,862,985 , GRCh37 chr5: 49,757,934-55,158,813 , NCBI36 chr5: 49,793,691-55,194,570 HMGB1P47, ITGA1, 72 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
    nsv3917640copy number variation1nstd102humanUncertain significance NCBI36 chr5: 54,359,842-55,271,282 , GRCh38 chr5: 55,028,257-55,939,697 , GRCh37 chr5: 54,324,085-55,235,525 MIR449C, GPX8, 24 more genes
    nsv3913817copy number variation1nstd102humanUncertain significance GRCh37 chr5: 45,566,963-55,802,320 , GRCh38 chr5: 45,566,861-56,506,493 , NCBI36 chr5: 45,602,720-55,838,077 LINC02118, ARL15, 90 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 LINC02241, ATPSCKMT, 878 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
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