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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5293467copy number variation1nstd204human GRCh38.p13 chr20: 62,966,101-64,149,200 , GRCh37.p13 chr20: 61,597,453-62,780,553 , ZGPAT, 72 more genes
    nsv5282963copy number variation1nstd204human GRCh38.p13 chr20: 63,863,001-64,088,600 , GRCh37.p13 chr20: 62,494,354-62,719,953 DNAJC5, RGS19, 22 more genes
    nsv4729772copy number variation1nstd102humanUncertain significance GRCh37 chr20: 62,576,747-62,915,555 , GRCh38.p12 chr20: 63,945,394-64,284,202 , GRCh38.p12 chr20|NT_187624.1: 1-183,433 NPBWR2, SOX18, 14 more genes
    nsv4729740copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,975,605-62,915,555 , GRCh38.p12 chr20: 63,344,253-64,284,202 STMN3, KCNQ2-AS1, 53 more genes
    nsv4676208copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,152,321-62,915,555 , GRCh38.p12 chr20: 62,555,114-64,284,202 GMEB2, LOC105372727, 94 more genes
    nsv4676181copy number variation1nstd102humanPathogenic GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052 LOC105372697, MIR647, 174 more genes
    nsv4676154copy number variation1nstd102humanLikely benign GRCh37 chr20: 62,678,394-62,884,479 , GRCh38.p12 chr20: 64,047,041-64,253,126 , GRCh38.p12 chr20|NT_187624.1: 1-161,717 LKAAEAR1, MIR6813, 7 more genes
    nsv4624780copy number variation1nstd183human GRCh37 chr20: 62,679,440-62,681,312 , GRCh38.p12 chr20: 64,048,087-64,049,959 SOX18, TCEA2
    nsv4619936copy number variation1nstd183human GRCh37 chr20: 62,535,216-62,746,667 , GRCh38.p12 chr20: 63,903,863-64,115,314 OPRL1, TCEA2, 20 more genes
    nsv4427452copy number variation1nstd174human GRCh37 chr20: 62,596,239-62,791,500 , GRCh38.p12 chr20: 63,964,886-64,160,147 SAMD10, SOX18, 10 more genes
    nsv4423339copy number variation1nstd174human GRCh37 chr20: 62,679,440-62,681,321 , GRCh38.p12 chr20: 64,048,087-64,049,968 TCEA2, SOX18
    nsv3966835insertion1nstd168human GRCh37.p13 chr20: 62,676,013-62,825,087 , GRCh38 chr20: 64,044,660-64,193,734 NPBWR2, MYT1, 7 more genes
    nsv3924353copy number variation1nstd102humanPathogenic NCBI36 chr20: 59,335,000-62,379,123 , GRCh38 chr20: 61,326,549-64,277,326 , GRCh37 chr20: 59,901,605-62,908,679 PPDPF, CRMA, 126 more genes
    nsv3922908copy number variation1nstd102humanPathogenic NCBI36 chr20: 61,010,752-62,435,964 , GRCh37.p13 chr20: 61,540,307-62,965,520 , GRCh38.p12 chr20: 62,908,955-64,334,167 NPBWR2, ZBTB46, 78 more genes
    nsv3922590copy number variation1nstd102humanPathogenic NCBI36 chr20: 60,553,022-62,343,283 , GRCh38 chr20: 62,545,370-64,241,486 , GRCh37 chr20: 61,142,577-62,872,839 RPL7P3, BHLHE23, 95 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3919856copy number variation1nstd102humanUncertain significance GRCh38 chr20: 63,827,808-64,100,279 , GRCh37 chr20: 62,459,161-62,731,632 , NCBI36 chr20: 61,929,605-62,202,076 C20orf181, MIR941-2, 24 more genes
    nsv3917244copy number variation1nstd102humanPathogenic NCBI36 chr20: 62,125,121-62,363,574 , GRCh37 chr20: 62,654,677-62,893,130 , GRCh38 chr20: 64,023,324-64,261,777 SOX18, MYT1, 10 more genes
    nsv3916789copy number variation1nstd102humanPathogenic GRCh37 chr20: 57,617,021-62,908,674 , GRCh38 chr20: 59,041,966-64,277,321 , NCBI36 chr20: 57,050,416-62,379,118 RNU7-141P, UCKL1, 153 more genes
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