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Items: 1 to 20 of 73

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7074105inversion1nstd229human GRCh38 chr10: 17,945,641-22,801,235 , GRCh37.p13 chr10: 18,252,931-23,090,164 UBE2V2P1, LOC105376450, 62 more genes
    nsv7063218inversion1nstd229human GRCh38 chr10: 21,664,813-22,447,089 , GRCh37.p13 chr10: 21,953,742-22,736,018 PSME2P6, LOC107984214, 16 more genes
    nsv6886506copy number variation1nstd229human GRCh38 chr10: 22,255,516-22,294,925 , GRCh37.p13 chr10: 22,544,445-22,583,854 LOC100130992, RPL31P45
    nsv6881977copy number variation1nstd229human GRCh38 chr10: 22,249,927-22,250,528 , GRCh37.p13 chr10: 22,538,856-22,539,457 LOC105376447, LOC100130992
    nsv6638019copy number variation1nstd102humanUncertain significance GRCh37 chr10: 22,208,767-23,220,277 , GRCh38.p12 chr10: 21,919,838-22,931,348 ADIPOR1P1, LINC03027, 19 more genes
    nsv6451911copy number variation1nstd223human GRCh38 chr10: 22,220,001-22,263,300 , GRCh37.p13 chr10: 22,508,930-22,552,229 LOC100130992, LOC105376447, 2 more genes
    nsv6446460copy number variation1nstd223human GRCh38 chr10: 22,247,001-22,256,300 , GRCh37.p13 chr10: 22,535,930-22,545,229 LOC100130992, LOC105376447
    nsv6440531copy number variation1nstd223human GRCh38 chr10: 22,232,001-22,375,900 , GRCh37.p13 chr10: 22,520,930-22,664,829 BMI1, RPL31P45, 5 more genes
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6132032copy number variation1nstd213human GRCh37 chr10: 21,540,000-22,750,001 , GRCh38.p12 chr10: 21,251,071-22,461,072 BMI1, MLLT10, 29 more genes
    nsv6132031copy number variation1nstd213human GRCh37 chr10: 18,100,000-28,260,001 , GRCh38.p12 chr10: 17,839,748-27,971,072 BMI1, CACNB2, 136 more genes
    nsv5493794copy number variation1nstd206human GRCh38 chr10: 22,255,442-22,255,540 , GRCh37.p13 chr10: 22,544,371-22,544,469 LOC100130992
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4176198copy number variation1nstd166human GRCh37.p13 chr10: 22,543,313-22,543,667 , GRCh38.p12 chr10: 22,254,384-22,254,738 LOC100130992, LOC105376447
    nsv3920796copy number variation1nstd102humanPathogenic NCBI36 chr10: 62,842-35,729,127 , GRCh37.p13 chr10: 72,842-35,689,121 , GRCh38.p12 chr10: 26,906-35,400,193 EPC1-AS1, RNU6-452P, 559 more genes
    nsv3920598copy number variation1nstd102humanBenign NCBI36 chr10: 4,636,926-47,125,152 , GRCh38 chr10: 4,604,734-48,074,662 , GRCh37 chr10: 4,646,926-47,531,169 LOC100420467, LOC105376474, 709 more genes
    nsv3917667copy number variation1nstd102humanPathogenic GRCh37 chr10: 224,406-26,628,907 , GRCh38 chr10: 90,205-26,339,978 , NCBI36 chr10: 126,145-26,668,913 RN7SKP241, DIP2C-AS1, 389 more genes
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