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Items: 1 to 20 of 120

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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
    nsv5946044copy number variation1nstd209human GRCh38 chr19: 19,126,719-19,129,819 , GRCh37.p13 chr19: 19,237,528-19,240,628 TMEM161A
    nsv5939701copy number variation1nstd209human GRCh38 chr19: 19,130,663-19,130,944 , GRCh37.p13 chr19: 19,241,472-19,241,753 TMEM161A
    nsv5876005copy number variation1nstd209human GRCh38 chr19: 19,126,748-19,129,797 , GRCh37.p13 chr19: 19,237,557-19,240,606 TMEM161A
    nsv5525736copy number variation1nstd206human GRCh38 chr19: 19,126,797-19,129,743 , GRCh37.p13 chr19: 19,237,606-19,240,552 TMEM161A
    nsv5519375copy number variation1nstd206human GRCh38 chr19: 19,121,875-19,121,963 , GRCh37.p13 chr19: 19,232,684-19,232,772 TMEM161A
    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
    nsv5288938copy number variation1nstd204human GRCh38.p13 chr19: 19,118,735-19,120,134 , GRCh37.p13 chr19: 19,229,544-19,230,943 TMEM161A
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014661copy number variation1nstd200human GRCh38 chr19: 19,127,478-19,128,535 , GRCh37.p13 chr19: 19,238,287-19,239,344 TMEM161A
    nsv5014660copy number variation1nstd200human GRCh38 chr19: 19,105,820-19,389,022 , GRCh37.p13 chr19: 19,216,629-19,499,831 TMEM161A, HAPLN4, 12 more genes
    nsv4860663copy number variation1nstd200human GRCh37 chr19: 19,238,374-19,239,201 , GRCh38.p12 chr19: 19,127,565-19,128,392 TMEM161A
    nsv4860662copy number variation1nstd200human GRCh37 chr19: 19,237,577-19,240,607 , GRCh38.p12 chr19: 19,126,768-19,129,798 TMEM161A
    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
    nsv4457454copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,230,490-19,440,304 , GRCh38.p12 chr19: 19,119,681-19,329,495 TM6SF2, NCAN, 10 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
    nsv4260270copy number variation1nstd166human GRCh37.p13 chr19: 19,228,383-19,228,467 , GRCh38.p12 chr19: 19,117,574-19,117,658 TMEM161A
    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
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