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Items: 1 to 20 of 87

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5299782copy number variation1nstd204human GRCh38.p13 chr19: 18,706,301-19,688,800 , GRCh37.p13 chr19: 18,817,111-19,799,609 , HOMER3-AS1, 37 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014668copy number variation1nstd200human GRCh38 chr19: 19,518,498-19,571,452 , GRCh37.p13 chr19: 19,629,307-19,682,261 YJEFN3, NDUFA13, 2 more genes
    nsv5014667copy number variation1nstd200human GRCh38 chr19: 19,512,643-19,936,068 , GRCh37.p13 chr19: 19,623,452-20,046,877 , GMIP, 20 more genes
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
    nsv4623010copy number variation1nstd183human GRCh37 chr19: 19,633,273-19,678,087 , GRCh38.p12 chr19: 19,522,464-19,567,278 NDUFA13, CILP2, 2 more genes
    nsv4457826copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,560,981-19,962,412 , GRCh38.p12 chr19: 19,450,172-19,851,603 ZNF56P, YJEFN3, 16 more genes
    nsv4436023complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 19,120,059-23,932,567 , GRCh37 chr19: 19,230,868-24,115,369 NCAN, BORCS8-MEF2B, 195 more genes
    nsv4272250copy number variation1nstd166human GRCh37.p13 chr19: 19,651,988-19,652,047 , GRCh38.p12 chr19: 19,541,179-19,541,238 CILP2
    nsv4265373copy number variation1nstd166human GRCh37.p13 chr19: 19,648,921-19,649,013 , GRCh38.p12 chr19: 19,538,112-19,538,204 CILP2
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 more genes
    nsv3921076copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,133,594-24,193,591 , GRCh37 chr19: 15,244,405-24,376,393 , NCBI36 chr19: 15,105,405-24,168,233 MRPL34, BNIP3P25, 358 more genes
    nsv3914228copy number variation1nstd102humanPathogenic NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054 LOC105372355, SUGP2, 411 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3908211copy number variation1nstd102humanLikely benign GRCh37 chr19: 19,651,060-19,657,440 , GRCh38.p12 chr19: 19,540,251-19,546,631 CILP2
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903399copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,644,501-19,657,440 , GRCh38.p12 chr19: 19,533,692-19,546,631 YJEFN3, CILP2
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 LENG8, SYDE1, 2408 more genes
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