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Items: 1 to 20 of 166

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6314514complex chromosomal rearrangement3nstd102humanPathogenic GRCh37 chr7: 128,114,023-128,114,023 , GRCh37 chr19: 29,247,464-29,247,464 , GRCh37 chr19: 29,247,464-29,247,464 , GRCh37 chr19: 32,861,768-32,861,768 , GRCh37 chr7: 128,114,028-128,114,028 , GRCh37 chr19: 32,861,768-32,861,768 , GRCh38.p12 chr7: 128,473,974-128,473,974 , GRCh38.p12 chr19: 28,756,557-28,756,557 , GRCh38.p12 chr19: 28,756,557-28,756,557 , GRCh38.p12 chr19: 32,370,862-32,370,862 , GRCh38.p12 chr19: 32,370,862-32,370,862 , GRCh38.p12 chr7: 128,473,969-128,473,969 ZNF507
    nsv3899090copy number variation1nstd102humanLikely benign GRCh37 chr12: 83,765,377-84,013,252 , GRCh38.p12 chr12: 83,371,598-83,619,473 LOC105369874
    nsv3898818copy number variation1nstd102humanLikely benign GRCh37 chr10: 128,328,611-128,544,207 , GRCh38.p12 chr10: 126,640,042-126,855,638 C10orf90
    nsv3900646copy number variation1nstd102humanLikely benign GRCh37 chr13: 85,909,019-86,064,348 , GRCh38.p12 chr13: 85,334,884-85,490,213 LINC00351
    nsv3894163copy number variation1nstd102humanLikely benign GRCh37 chr18: 34,546,490-34,698,627 , GRCh38.p12 chr18: 36,966,527-37,118,664 KIAA1328
    nsv3886575copy number variation1nstd102humanLikely benign GRCh37 chr5: 131,145,181-131,266,601 , GRCh38.p12 chr5: 131,809,488-131,930,908 MEIKIN
    nsv3903155copy number variation1nstd102humanLikely benign GRCh37 chr13: 29,714,684-29,828,112 , GRCh38.p12 chr13: 29,140,547-29,253,975 MTUS2
    nsv3887427copy number variation1nstd102humanLikely benign GRCh37 chr3: 76,848,167-76,951,689 , GRCh38.p12 chr3: 76,799,016-76,902,538 ROBO2
    nsv3902243copy number variation1nstd102humanLikely benign GRCh37 chr11: 40,567,422-40,660,470 , GRCh38.p12 chr11: 40,545,872-40,638,920 LRRC4C
    nsv3882011copy number variation1nstd102humanLikely benign GRCh37 chr3: 134,978,716-135,053,549 , GRCh38.p12 chr3: 135,259,874-135,334,707 EPHB1
    nsv3896610copy number variation1nstd102humanLikely benign GRCh37 chr9: 9,919,638-9,990,269 , GRCh38.p12 chr9: 9,919,638-9,990,269 PTPRD
    nsv3898270copy number variation1nstd102humanBenign GRCh37 chr16: 84,429,584-84,490,643 , GRCh38.p12 chr16: 84,395,978-84,457,037 ATP2C2
    nsv3890129copy number variation1nstd102humanLikely benign GRCh37 chr8: 10,447,116-10,504,819 , GRCh38.p12 chr8: 10,589,606-10,647,309 , GRCh38.p12 chr8|NW_018654717.1: 2,699,773-2,757,432 RP1L1
    nsv3889078copy number variation1nstd102humanLikely benign GRCh37 chr2: 39,982,433-40,037,717 , GRCh38.p12 chr2: 39,755,293-39,810,577 THUMPD2
    nsv3873989copy number variation1nstd102humanBenign GRCh37 chr3: 85,561,190-85,612,793 , GRCh38.p12 chr3: 85,512,040-85,563,643 CADM2
    nsv3908056copy number variation1nstd102humanBenign GRCh37 chr11: 99,519,242-99,568,648 , GRCh38.p12 chr11: 99,648,511-99,697,917 CNTN5
    nsv3909639copy number variation1nstd102humanBenign GRCh37 chr20: 15,062,923-15,103,156 , GRCh38.p12 chr20: 15,082,277-15,122,510 MACROD2
    nsv3904305copy number variation1nstd102humanLikely benign GRCh37 chr20: 4,931,970-4,972,088 , GRCh38.p12 chr20: 4,951,324-4,991,442 SLC23A2
    nsv3890721copy number variation1nstd102humanLikely benign GRCh37 chr8: 71,608,781-71,646,728 , GRCh38.p12 chr8: 70,696,546-70,734,493 XKR9
    nsv3881452copy number variation1nstd102humanBenign GRCh37 chr2: 133,927,604-133,963,658 , GRCh38.p12 chr2: 133,170,032-133,206,086 NCKAP5
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