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Items: 1 to 20 of 25

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4675723copy number variation1nstd102humanUncertain significance GRCh37 chr10: 35,683,004-35,802,261 , GRCh38.p12 chr10: 35,394,076-35,513,333 CCNY
    nsv4455994copy number variation1nstd102humanUncertain significance GRCh37 chr10: 35,666,405-35,757,646 , GRCh38.p12 chr10: 35,377,477-35,468,718 CCNY
    nsv4457194copy number variation1nstd102humanUncertain significance GRCh37 chr10: 35,737,017-35,793,136 , GRCh38.p12 chr10: 35,448,089-35,504,208 CCNY
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 CCNY, RNU7-12P, 1876 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 CCNY, LOC100419870, 2105 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 CCNY, AGAP14P, 2097 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 CCNY, ANXA11, 2085 more genes
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 CCNY, TUBB8, 2085 more genes
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 CCNY, EXOC6, 1906 more genes
    nsv3904390copy number variation1nstd102humanPathogenic GRCh37 chr10: 100,026-50,961,640 , GRCh38.p12 chr10: 54,086-49,753,594 CCNY, LINC00700, 806 more genes
    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 CCNY, EPC1-AS1, 559 more genes
    nsv3914331copy number variation1nstd102humanPathogenic NCBI36 chr10: 32,328,854-38,448,615 , GRCh38 chr10: 31,999,920-38,119,681 , GRCh37 chr10: 32,288,848-38,408,609 CCNY, VN1R53P, 87 more genes
    nsv3923244copy number variation1nstd102humanPathogenic GRCh38 chr10: 34,686,264-35,684,215 , GRCh37 chr10: 34,975,192-35,973,143 , NCBI36 chr10: 35,015,198-36,013,149 CCNY, SS18L2P1, 20 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 CCNY, LOC100420467, 709 more genes
    nsv3906005copy number variation1nstd102humanLikely benign GRCh37 chr10: 35,052,688-35,724,594 , GRCh38.p12 chr10: 34,763,760-35,435,666 CCNY, MIR3611, 15 more genes
    nsv3897575copy number variation1nstd102humanLikely benign GRCh37 chr10: 35,021,066-35,594,219 , GRCh38.p12 chr10: 34,732,138-35,305,291 CCNY, RNU6-847P, 15 more genes
    nsv3904916copy number variation1nstd102humanBenign GRCh37 chr10: 35,207,822-35,554,947 , GRCh38.p12 chr10: 34,918,894-35,266,019 CCNY, PRDX2P2, 11 more genes
    nsv3884932copy number variation1nstd102humanUncertain significance GRCh38 chr10: 33,254,302-35,641,435 , GRCh37 chr10: 33,543,230-35,930,363 CCNY, RPL37P18, 29 more genes
    nsv4456345copy number variation1nstd102humanUncertain significance GRCh37 chr10: 34,795,319-36,729,226 , GRCh38.p12 chr10: 34,506,391-36,440,298 CCNY, LOC107984220, 29 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 CCNY, C1QL3, 774 more genes
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