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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147717copy number variation1nstd232human GRCh37.p13 chr19: 39,879,315-39,879,399 , GRCh38.p12 chr19: 39,388,675-39,388,759 PAF1, SAMD4B
    nsv7147494copy number variation1nstd232human GRCh37.p13 chr19: 39,879,837-39,879,919 , GRCh38.p12 chr19: 39,389,197-39,389,279 PAF1, SAMD4B
    nsv7144822copy number variation1nstd232human GRCh37.p13 chr19: 39,879,105-39,879,196 , GRCh38.p12 chr19: 39,388,465-39,388,556 PAF1, SAMD4B
    nsv7144630insertion1nstd232human GRCh37.p13 chr19: 39,877,442-39,877,442 , GRCh38.p12 chr19: 39,386,802-39,386,802 PAF1, SAMD4B
    nsv7138105copy number variation1nstd232human GRCh37.p13 chr19: 39,877,043-39,877,120 , GRCh38.p12 chr19: 39,386,403-39,386,480 PAF1, SAMD4B
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7075514inversion1nstd229human GRCh38 chr19: 38,994,526-39,502,034 , GRCh37.p13 chr19: 39,485,166-39,992,674 RPS16, PLEKHG2, 25 more genes
    nsv7071361inversion1nstd229human GRCh38 chr19: 39,004,066-42,402,005 , GRCh37.p13 chr19: 39,494,706-42,906,157 RAB4B, RABAC1, 160 more genes
    nsv7068288inversion1nstd229human GRCh38 chr19: 39,023,970-42,945,419 , GRCh37.p13 chr19: 39,514,610-43,449,571 MIR4530, RNU6-195P, 178 more genes
    nsv7008627copy number variation1nstd229human GRCh38 chr19: 39,364,901-39,554,300 , GRCh37.p13 chr19: 39,855,541-40,044,940 CRIPTOP7, ZFP36, 16 more genes
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5944000copy number variation1nstd209human GRCh38 chr19: 39,387,653-39,412,021 , GRCh37.p13 chr19: 39,878,293-39,902,661 ZFP36, PAF1, 5 more genes
    nsv5873243copy number variation1nstd209human GRCh38 chr19: 39,390,235-39,395,534 , GRCh37.p13 chr19: 39,880,875-39,886,174 MED29, PAF1, 1 more genes
    nsv5281379copy number variation1nstd204human GRCh38.p13 chr19: 39,383,501-39,387,200 , GRCh37.p13 chr19: 39,874,141-39,877,840 PAF1, SAMD4B
    nsv4628819copy number variation1nstd183human GRCh37 chr19: 39,811,570-39,886,212 , GRCh38.p12 chr19: 39,320,930-39,395,572 GMFG, PAF1, 4 more genes
    nsv4624865copy number variation1nstd183human GRCh37 chr19: 39,881,236-39,904,463 , GRCh38.p12 chr19: 39,390,596-39,413,823 ZFP36, PAF1, 5 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
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