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Items: 13

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    Number of Variants: 13

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3881804copy number variation1nstd102humanBenign GRCh37 chr6: 53,504,277-53,517,035 , GRCh38.p12 chr6: 53,639,479-53,652,237 KLHL31
    nsv3923721copy number variation1nstd102humanPathogenic GRCh38 chr6: 45,681,671-54,212,044 , GRCh37 chr6: 45,649,408-54,076,842 , NCBI36 chr6: 45,757,386-54,184,801 KLHL31, PAQR8, 131 more genes
    nsv3922315copy number variation1nstd102humanPathogenic GRCh37 chr6: 50,938,895-57,297,586 , NCBI36 chr6: 51,046,854-57,405,545 , GRCh38 chr6: 50,971,182-57,432,788 KLHL31, MLIP-AS1, 100 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 KLHL31, LOC105378061, 2914 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 KLHL31, RNU6-411P, 2910 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 KLHL31, SOD1P1, 2905 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 KLHL31, ITPR3, 2905 more genes
    nsv4350067copy number variation1nstd102humanPathogenic GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650 KLHL31, HLA-DPB2, 1001 more genes
    nsv3910455copy number variation1nstd102humanPathogenic GRCh37 chr6: 51,061,467-53,724,432 , GRCh38 chr6: 51,093,754-53,859,634 , NCBI36 chr6: 51,169,426-53,832,391 KLHL31, LOC101927082, 58 more genes
    nsv4729270copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 48,626,041-55,575,545 , GRCh38.p12 chr6: 48,658,305-55,710,747 KLHL31, CRISP1, 105 more genes
    nsv6314749copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 43,636,308-64,947,206 , GRCh38.p12 chr6: 43,668,571-64,237,313 KLHL31, ACTG1P9, 245 more genes
    nsv6638066copy number variation1nstd102humanUncertain significance GRCh38 chr6: 53,151,508-58,400,428 , GRCh37.p13 chr6: 53,016,306-58,726,706 KLHL31, NPM1P36, 73 more genes
    nsv4729393copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,657,712-53,622,715 , GRCh38.p12 chr6: 52,792,914-53,757,917 KLHL31, KILH, 29 more genes
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