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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5348033translocation1nstd200human GRCh38 chr10: 97,772,172-97,772,172 , GRCh38 chr10: 97,772,232-97,772,232 , GRCh37.p13 chr10: 99,531,929-99,531,929 , GRCh37.p13 chr10: 99,531,989-99,531,989 SFRP5
    nsv4973951copy number variation1nstd200human GRCh38 chr10: 97,671,807-97,847,606 , GRCh37.p13 chr10: 99,431,564-99,607,363 LOC107984260, GOLGA7B-DT, 5 more genes
    nsv4973950copy number variation1nstd200human GRCh38 chr10: 97,654,562-97,781,768 , GRCh37.p13 chr10: 99,414,319-99,541,525 MARVELD1, AVPI1, 3 more genes
    nsv4833405copy number variation1nstd200human GRCh37 chr10: 99,431,564-99,607,363 , GRCh38.p12 chr10: 97,671,807-97,847,606 SFRP5, PI4K2A, 5 more genes
    nsv4605815copy number variation1nstd183human GRCh37 chr10: 99,469,608-99,526,507 , GRCh38.p12 chr10: 97,709,851-97,766,750 SFRP5, MARVELD1, 1 more genes
    nsv4344602sequence alteration1nstd166human GRCh37.p13 chr10: 99,530,054-99,533,652 , GRCh38.p12 chr10: 97,770,297-97,773,895 SFRP5
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv4173720copy number variation1nstd166human GRCh37.p13 chr10: 99,448,836-99,636,627 , GRCh38.p12 chr10: 97,689,079-97,876,870 SFRP5, CRTAC1, 6 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3911437copy number variation1nstd102humanPathogenic GRCh38 chr10: 93,181,201-101,356,779 , NCBI36 chr10: 94,930,948-103,106,526 , GRCh37 chr10: 94,940,958-103,116,536 SLF2, CUTC, 171 more genes
    nsv3909942copy number variation1nstd102humanPathogenic GRCh37 chr10: 96,872,364-118,383,651 , GRCh38 chr10: 95,112,607-116,776,637 , NCBI36 chr10: 96,862,354-118,526,138 LOC102723665, SFR1, 360 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 SHOC2, FAM245B, 1487 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3905489copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639 LOC105378476, SMC3, 688 more genes
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
    nsv3894905copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,476,328-99,552,148 , GRCh38.p12 chr10: 97,716,571-97,792,391 MARVELD1, ZFYVE27, 1 more genes
    nsv3894877copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,908,171-101,809,723 , GRCh38.p12 chr10: 92,148,414-100,049,966 RNY3P12, ANKRD2, 146 more genes
    nsv3894450copy number variation1nstd102humandrug response GRCh37 chr10: 85,557,432-105,804,295 , GRCh38.p12 chr10: 83,797,676-104,044,537 HPS1, LOC112268063, 422 more genes
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