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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3895275copy number variation1nstd102humanBenign GRCh37 chr7: 131,387,145-131,395,704 , GRCh38.p12 chr7: 131,702,386-131,710,945 RPS15AP22
    nsv3874890copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 72,503,642-72,716,038 , GRCh38.p12 chr2: 72,276,513-72,488,909 EXOC6B, RPS15AP13
    nsv3898976copy number variation1nstd102humanLikely pathogenic NCBI36 chrX: 41,480,810-41,551,609 , GRCh37 chrX: 41,595,866-41,666,665 , GRCh38 chrX: 41,736,613-41,807,412 CASK, RPS15AP39
    nsv3909681copy number variation1nstd102humanBenign GRCh37 chr14: 47,855,051-48,037,380 , GRCh38.p12 chr14: 47,385,848-47,568,177 RPS15AP3, MDGA2
    nsv3871396copy number variation1nstd102humanBenign GRCh37 chr1: 62,638,306-62,657,186 , GRCh38.p12 chr1: 62,172,634-62,191,514 RPS15AP7, PIGPP2
    nsv3874267copy number variation1nstd102humanBenign GRCh37 chr1: 62,642,163-62,657,186 , GRCh38.p12 chr1: 62,176,491-62,191,514 PIGPP2, RPS15AP7
    nsv3884771copy number variation1nstd102humanBenign GRCh37 chr1: 62,644,118-62,657,063 , GRCh38.p12 chr1: 62,178,446-62,191,391 RPS15AP7, PIGPP2
    nsv3877025copy number variation1nstd102humanBenign GRCh37 chr1: 62,646,182-62,657,530 , GRCh38.p12 chr1: 62,180,510-62,191,858 RPS15AP7, PIGPP2
    nsv3875013copy number variation1nstd102humanBenign GRCh37 chr1: 62,646,182-62,657,186 , GRCh38.p12 chr1: 62,180,510-62,191,514 PIGPP2, RPS15AP7
    nsv3888457copy number variation1nstd102humanBenign GRCh37 chr1: 62,646,182-62,657,063 , GRCh38.p12 chr1: 62,180,510-62,191,391 PIGPP2, RPS15AP7
    nsv3874963copy number variation1nstd102humanBenign GRCh37 chr1: 62,654,877-62,657,186 , GRCh38.p12 chr1: 62,189,205-62,191,514 PIGPP2, RPS15AP7
    nsv3891430copy number variation1nstd102humanBenign GRCh37 chr16: 63,297,445-63,396,075 , GRCh38.p12 chr16: 63,263,541-63,362,171 LOC105371308, RPS15AP34
    nsv3908239copy number variation1nstd102humanBenign GRCh37 chr16: 63,297,445-63,394,718 , GRCh38.p12 chr16: 63,263,541-63,360,814 RPS15AP34, LOC105371308
    nsv3922055copy number variation1nstd102humanBenign NCBI36 chr6: 35,597,487-35,646,122 , GRCh37 chr6: 35,489,509-35,538,144 , GRCh38 chr6: 35,521,732-35,570,367 LOC101929309, RPS15AP19
    nsv3918958copy number variation1nstd102humanBenign/Likely benign NCBI36 chr6: 35,623,754-35,646,122 , GRCh37 chr6: 35,515,776-35,538,144 , GRCh38 chr6: 35,547,999-35,570,367 RPS15AP19, LOC101929309
    nsv4456565copy number variation1nstd102humanUncertain significance GRCh37 chr7: 132,986,377-133,391,921 , GRCh38.p12 chr7: 133,301,623-133,707,168 RPS15AP23, EXOC4
    nsv3921190copy number variation1nstd102humanUncertain significance NCBI36 chr7: 132,639,101-133,016,077 , GRCh37 chr7: 132,988,561-133,365,537 , GRCh38 chr7: 133,303,807-133,680,784 RPS15AP23, EXOC4
    nsv3918393copy number variation1nstd102humanUncertain significance NCBI36 chr16: 61,878,482-62,024,709 , GRCh37.p13 chr16: 63,320,981-63,467,208 , GRCh38.p12 chr16: 63,287,077-63,433,304 RPS15AP34, LOC105371308
    nsv3923474copy number variation1nstd102humanUncertain significance NCBI36 chr16: 61,910,485-62,052,192 , GRCh37.p13 chr16: 63,352,984-63,494,691 , GRCh38.p12 chr16: 63,319,080-63,460,787 LOC105371308, RPS15AP34
    nsv4675578copy number variation1nstd102humanUncertain significance GRCh37 chr7: 132,977,705-133,104,509 , GRCh38.p12 chr7: 133,292,951-133,419,755 RPS15AP23, EXOC4
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