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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5527137copy number variation1nstd206human GRCh38 chr20: 23,428,335-23,589,000 , GRCh37.p13 chr20: 23,408,972-23,569,637 CST8, CSTL1, 6 more genes
    nsv5021766copy number variation1nstd200human GRCh38 chr20: 23,567,234-23,570,275 , GRCh37.p13 chr20: 23,547,871-23,550,912 CST9L
    nsv4862363copy number variation1nstd200human GRCh37 chr20: 23,547,871-23,550,912 , GRCh38.p12 chr20: 23,567,234-23,570,275 CST9L
    nsv4729864copy number variation1nstd102humanLikely benign GRCh37 chr20: 23,413,239-23,569,271 , GRCh38.p12 chr20: 23,432,602-23,588,634 CST8, CSTL1, 6 more genes
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
    nsv4535189copy number variation1nstd166human GRCh37.p13 chr20: 23,411,998-23,571,000 , GRCh38.p12 chr20: 23,431,361-23,590,363 CST8, CSTL1, 6 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    nsv4336704sequence alteration1nstd166human GRCh37.p13 chr20: 8,105,854-23,795,733 , GRCh38.p12 chr20: 8,125,207-23,815,096 , BFSP1, 242 more genes
    nsv4279744copy number variation1nstd166human GRCh37.p13 chr20: 23,374,022-24,054,368 , GRCh38.p12 chr20: 23,393,385-24,073,731 , CST3, 23 more genes
    nsv4275080copy number variation1nstd166human GRCh37.p13 chr20: 23,541,600-23,550,001 , GRCh38.p12 chr20: 23,560,963-23,569,364 CST9L
    nsv4273259copy number variation1nstd166human GRCh37.p13 chr20: 23,547,871-23,550,912 , GRCh38.p12 chr20: 23,567,234-23,570,275 CST9L
    nsv3922272copy number variation1nstd102humanPathogenic GRCh38 chr20: 80,106-30,227,427 , NCBI36 chr20: 8,747-28,075,764 , GRCh37 chr20: 60,747-29,462,103 ISM1-AS1, CST2, 498 more genes
    nsv3921497copy number variation1nstd102humanUncertain significance GRCh38 chr20: 23,455,996-24,050,737 , GRCh37 chr20: 23,436,633-24,031,374 , NCBI36 chr20: 23,384,633-23,979,374 CSTP1, CST9LP2, 19 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
    nsv3919898copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38 chr20: 80,927-26,324,843 , NCBI36 chr20: 9,568-26,253,479 MIR3192, CFAP61, 473 more genes
    nsv3913796copy number variation1nstd102humanPathogenic NCBI36 chr20: 18,580-28,133,653 , GRCh37.p13 chr20: 70,580-29,519,992 , GRCh38.p12 chr20: 89,939-30,285,316 RNY4P11, EIF4E2P1, 500 more genes
    nsv3913704copy number variation1nstd102humanPathogenic GRCh38 chr20: 89,939-25,697,564 , NCBI36 chr20: 18,580-25,626,200 , GRCh37 chr20: 70,580-25,678,200 NRSN2, LOC102724545, 459 more genes
    nsv3913354copy number variation1nstd102humanPathogenic GRCh38 chr20: 22,061,586-30,285,812 , GRCh37 chr20: 22,042,224-29,520,488 , NCBI36 chr20: 21,990,224-28,134,149 LOC391239, AGGF1P10, 127 more genes
    nsv3911410copy number variation1nstd102humanUncertain significance NCBI36 chr20: 23,345,095-23,524,189 , GRCh37.p13 chr20: 23,397,095-23,576,189 , GRCh38.p12 chr20: 23,416,458-23,595,552 CST12P, CST8, 7 more genes
    nsv3910142copy number variation1nstd102humanPathogenic GRCh37 chr20: 9,792,081-37,945,599 , GRCh38 chr20: 9,811,433-39,316,956 , NCBI36 chr20: 9,740,081-37,379,013 DYNLRB1, LOC107985402, 555 more genes
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