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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960629copy number variation1nstd209human GRCh38 chr20: 24,517,514-25,490,454 , GRCh37.p13 chr20: 24,498,150-25,471,090 LOC105372581, LOC107985402, 18 more genes
    nsv5529010copy number variation1nstd206human GRCh38 chr20: 24,494,187-25,093,208 , GRCh37.p13 chr20: 24,474,823-25,073,844 CST7, VSX1, 6 more genes
    nsv5328364translocation1nstd204human GRCh38.p13 chr20: 25,072,848-25,072,848 , GRCh38.p13 chr20: 25,072,559-25,072,559 , GRCh37.p13 chr20: 25,053,195-25,053,195 , GRCh37.p13 chr20: 25,053,484-25,053,484 VSX1
    nsv5021823copy number variation1nstd200human GRCh38 chr20: 25,047,890-25,075,094 , GRCh37.p13 chr20: 25,028,526-25,055,730 ACSS1, VSX1
    nsv4862401copy number variation1nstd200human GRCh37 chr20: 25,053,195-25,053,484 , GRCh38.p12 chr20: 25,072,559-25,072,848 VSX1
    nsv4729921copy number variation1nstd102humanUncertain significance GRCh37 chr20: 24,989,180-25,156,722 , GRCh38.p12 chr20: 25,008,544-25,176,086 VSX1, LOC391239, 3 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
    nsv4457450copy number variation1nstd102humanUncertain significance GRCh37 chr20: 24,232,978-25,520,939 , GRCh38.p12 chr20: 24,252,342-25,540,303 LOC284798, NINL, 21 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
    nsv4282337copy number variation1nstd166human GRCh37.p13 chr20: 24,995,893-26,182,641 , GRCh38.p12 chr20: 25,015,257-26,202,005 LOC105372579, FAM182A, 32 more genes
    nsv4272813copy number variation1nstd166human GRCh37.p13 chr20: 25,049,074-25,049,433 , GRCh38.p12 chr20: 25,068,438-25,068,797 VSX1
    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
    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
    nsv3919409copy number variation1nstd102humanUncertain significance NCBI36 chr20: 24,784,840-25,703,040 , GRCh37.p13 chr20: 24,836,840-25,755,040 , GRCh38.p12 chr20: 24,856,204-25,774,404 ENTPD6, LOC105372581, 26 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
    nsv3911650copy number variation1nstd102humanUncertain significance NCBI36 chr20: 24,960,315-25,554,156 , GRCh38 chr20: 25,031,679-25,625,520 , GRCh37 chr20: 25,012,315-25,606,156 PPIAP2, VSX1, 15 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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