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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7033847copy number variation1nstd229human GRCh38 chr20: 22,983,108-23,366,927 , GRCh37.p13 chr20: 22,963,745-23,347,564 GZF1, CD93, 10 more genes
    nsv7028713copy number variation1nstd229human GRCh38 chr20: 22,899,137-23,319,697 , GRCh37.p13 chr20: 22,879,775-23,300,334 LOC101929707, RNA5SP478, 9 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6134281copy number variation1nstd213human GRCh37 chr20: 22,780,000-23,230,001 , GRCh38.p12 chr20: 22,799,362-23,249,364 SSTR4, THBD, 9 more genes
    nsv6134280copy number variation1nstd213human GRCh37 chr20: 22,530,000-23,650,001 , GRCh38.p12 chr20: 22,549,362-23,669,364 CST3, CYB5AP4, 33 more genes
    nsv6134279copy number variation1nstd213human GRCh37 chr20: 22,140,000-23,520,001 , GRCh38.p12 chr20: 22,159,362-23,539,364 RNA5SP478, LNCNEF, 34 more genes
    nsv6134275copy number variation1nstd213human GRCh37 chr20: 19,430,000-23,860,001 , GRCh38.p12 chr20: 19,449,356-23,879,364 CST1, CST4, 87 more genes
    nsv6133908copy number variation1nstd213human GRCh37 chr20: 23,010,000-23,580,001 , GRCh38.p12 chr20: 23,029,363-23,599,364 SSTR4, THBD, 20 more genes
    nsv4862352copy number variation1nstd200human GRCh37 chr20: 23,015,923-23,015,995 , GRCh38.p12 chr20: 23,035,286-23,035,358 SSTR4
    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
    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
    nsv4276734copy number variation1nstd166human GRCh37.p13 chr20: 22,879,833-23,300,334 , GRCh38.p12 chr20: 22,899,195-23,319,697 LOC100419956, LOC107985449, 9 more genes
    nsv3962591insertion1nstd168human GRCh38 chr20: 23,014,423-23,051,380 , GRCh37.p13 chr20: 22,995,060-23,032,017 SSTR4, THBD, 1 more genes
    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
    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
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