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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903839copy number variation1nstd209human GRCh38 chr5: 79,180,365-84,539,350 , GRCh37.p13 chr5: 78,476,188-83,835,168 , ANKRD34B, 84 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4948961copy number variation1nstd200human GRCh38 chr5: 83,281,087-83,442,299 , GRCh37.p13 chr5: 82,576,906-82,738,118 LOC105379053, FTH1P9, 2 more genes
    nsv4805627copy number variation1nstd200human GRCh37 chr5: 82,576,906-82,738,118 , GRCh38.p12 chr5: 83,281,087-83,442,299 COQ10BP2, XRCC4, 2 more genes
    nsv4675667copy number variation1nstd102humanPathogenic GRCh37 chr5: 72,790,061-97,478,870 , GRCh38.p12 chr5: 73,494,236-98,143,166 LOC101929380, LIX1-AS1, 318 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
    nsv4328126inversion1nstd166human GRCh37.p13 chr5: 75,669,511-101,876,780 , GRCh38.p12 chr5: 76,373,686-102,541,076 , BHMT, 331 more genes
    nsv3969386copy number variation1nstd168human GRCh38 chr5: 83,212,419-83,282,446 , GRCh37.p13 chr5: 82,508,238-82,578,265 COQ10BP2, XRCC4
    nsv3923657copy number variation1nstd102humanLikely benign NCBI36 chr5: 82,243,098-83,063,511 , GRCh37.p13 chr5: 82,207,342-83,027,755 , GRCh38.p12 chr5: 82,911,523-83,731,936 VCAN-AS1, ST13P12, 14 more genes
    nsv3917856copy number variation1nstd102humanPathogenic GRCh38 chr5: 74,163,186-110,809,453 , NCBI36 chr5: 73,494,767-110,173,052 , GRCh37 chr5: 73,459,011-110,145,153 CSNK1A1P3, POLR3G, 413 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
    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
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    nsv3884600copy number variation1nstd102humanUncertain significance GRCh37 chr5: 82,355,242-82,603,880 , GRCh38.p12 chr5: 83,059,423-83,308,061 COQ10BP2, TMEM167A, 3 more genes
    nsv3880689copy number variation1nstd102humanUncertain significance GRCh37 chr5: 82,095,432-82,688,973 , GRCh38.p12 chr5: 82,799,613-83,393,154 XRCC4, LINC01338, 10 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SPEF2, NDST1, 2490 more genes
    nsv3875052copy number variation1nstd102humanUncertain significance GRCh37 chr5: 82,207,342-82,631,072 , GRCh38.p12 chr5: 82,911,523-83,335,253 RPL13P9, TMEM167A, 7 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 PCDHGC5, RGS14, 2492 more genes
    nsv3134576copy number variation2nstd151human GRCh37 chr5: 82,554,346-82,649,066 , GRCh38.p12 chr5: 83,258,527-83,353,247 XRCC4, COQ10BP2
    nsv2787306copy number variation1nstd132human NCBI36 chr5: 82,550,284-82,715,894 , GRCh37.p13 chr5: 82,514,528-82,680,138 , GRCh38.p12 chr5: 83,218,709-83,384,319 XRCC4, COQ10BP2
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