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Items: 1 to 20 of 106

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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
    nsv5289668copy number variation1nstd204human GRCh37.p13 chr19: 18,552,711-18,764,410 , GRCh38.p13 chr19: 18,441,901-18,653,600 UBA52, ELL, 7 more genes
    nsv5282384copy number variation1nstd204human GRCh38.p13 chr19: 18,292,801-18,706,100 , GRCh37.p13 chr19: 18,403,611-18,816,910 ELL, FKBP8, 17 more genes
    nsv5194433mobile element insertion1nstd203human GRCh38 chr19: 18,612,368-18,612,384 , GRCh37.p13 chr19: 18,723,178-18,723,194 TMEM59L
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 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
    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
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    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
    nsv3901919copy number variation1nstd102humanBenign GRCh37 chr19: 18,637,610-18,740,208 , GRCh38.p12 chr19: 18,526,800-18,629,398 FKBP8, CRLF1, 4 more genes
    nsv3895942copy number variation1nstd102humanPathogenic GRCh37 chr19: 16,526,787-24,631,604 , GRCh38.p12 chr19: 16,415,976-24,448,802 BNIP3P37, ZNF675, 307 more genes
    nsv3168589copy number variation1nstd158human GRCh38.p12 chr19: 18,471,384-18,675,925 , GRCh37 chr19: 18,582,194-18,786,735 UBA52, ELL, 7 more genes
    nsv3158672copy number variation1nstd151human GRCh37 chr19: 18,731,215-18,780,087 , GRCh38.p12 chr19: 18,620,405-18,669,277 RN7SL155P, KLHL26, 1 more genes
    nsv2784918copy number variation1nstd132human NCBI36 chr19: 18,561,047-18,955,226 , GRCh37.p13 chr19: 18,700,047-19,094,226 , GRCh38.p12 chr19: 18,589,237-18,983,417 , COMP, 15 more genes
    nsv2783993copy number variation1nstd132human NCBI36 chr19: 18,428,039-18,955,226 , GRCh37.p13 chr19: 18,567,039-19,094,226 , GRCh38.p12 chr19: 18,456,229-18,983,417 , COMP, 19 more genes
    nsv2768219copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr19: 260,911-20,692,745 , GRCh37 chr19: 260,911-20,875,551 , ACP5, 914 more genes
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