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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556834sequence alteration1nstd206human GRCh38 chr19: 23,310,120-23,985,140 , GRCh37.p13 chr19: 23,492,922-24,167,942 ZNF681, VN1R92P, 21 more genes
    nsv5530175copy number variation1nstd206human GRCh38 chr19: 22,813,931-23,470,653 , GRCh37.p13 chr19: 22,996,733-23,653,455 VN1R92P, ZNF730, 23 more genes
    nsv5014751copy number variation1nstd200human GRCh38 chr19: 23,356,288-23,767,969 , GRCh37.p13 chr19: 23,539,090-23,950,771 LOC105372338, BNIP3P8, 16 more genes
    nsv5014744copy number variation1nstd200human GRCh38 chr19: 23,128,275-24,410,482 , GRCh37.p13 chr19: 23,311,077-24,593,284 BNIP3P8, ZNF675, 34 more genes
    nsv4865049copy number variation1nstd200human GRCh37 chr19: 23,539,090-23,950,771 , GRCh38.p12 chr19: 23,356,288-23,767,969 LOC105372339, RPSA2, 16 more genes
    nsv4680028copy number variation1nstd189human GRCh37.p13 chr19: 22,675,451-24,584,093 , GRCh38.p12 chr19: 22,492,649-24,401,291 ZNF726P1, ZNF91, 60 more genes
    nsv4676147copy number variation1nstd102humanUncertain significance GRCh37 chr19: 22,630,650-24,487,350 , GRCh38.p12 chr19: 22,447,848-24,304,548 ZNF726P1, LOC105372334, 64 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
    nsv4367465copy number variation1nstd173human GRCh37 chr19: 23,538,866-23,857,848 , GRCh38.p12 chr19: 23,356,064-23,675,046 LOC100131479, LOC105372338, 13 more genes
    nsv4334827sequence alteration1nstd166human GRCh37.p13 chr19: 23,492,926-24,167,901 , GRCh38.p12 chr19: 23,310,124-23,985,099 ZNF675, ZNF726, 21 more genes
    nsv4254624copy number variation1nstd166human GRCh37.p13 chr19: 23,566,703-23,566,766 , GRCh38.p12 chr19: 23,383,901-23,383,964 ZNF91, CDC42EP3P1
    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
    nsv3909053copy number variation1nstd102humanLikely benign GRCh37 chr19: 22,635,439-24,505,637 , GRCh38.p12 chr19: 22,452,637-24,322,835 RN7SL860P, LINC01224, 63 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
    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
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