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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5908846copy number variation1nstd209human GRCh38 chr10: 89,591,029-89,591,082 , GRCh37.p13 chr10: 91,350,786-91,350,839 MIR107, PANK1
    nsv5480198copy number variation1nstd206human GRCh38 chr10: 89,591,029-89,591,084 , GRCh37.p13 chr10: 91,350,786-91,350,841 MIR107, PANK1
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4973877copy number variation1nstd200human GRCh38 chr10: 89,366,953-89,877,440 , GRCh37.p13 chr10: 91,126,710-91,637,197 SLC16A12-AS1, LINC00865, 14 more genes
    nsv4833445copy number variation1nstd200human GRCh37 chr10: 91,126,710-91,637,197 , GRCh38.p12 chr10: 89,366,953-89,877,440 SLC16A12, PANK1, 14 more genes
    nsv4729624copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,685,387-92,144,296 , GRCh38.p12 chr10: 86,925,630-90,384,539 LOC105378414, RN7SL78P, 84 more genes
    nsv4681131copy number variation1nstd102humanPathogenic GRCh37 chr10: 91,098,418-91,371,805 , GRCh38.p12 chr10: 89,338,661-89,612,048 MIR107, PANK1, 9 more genes
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4178603copy number variation1nstd166human GRCh37.p13 chr10: 91,350,786-91,350,841 , GRCh38.p12 chr10: 89,591,029-89,591,084 PANK1, MIR107
    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
    nsv3912267copy number variation1nstd102humanUncertain significance NCBI36 chr10: 90,845,025-91,383,281 , GRCh38 chr10: 89,095,288-89,633,544 , GRCh37 chr10: 90,855,045-91,393,301 SLC16A12-AS1, PANK1, 15 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
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 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
    nsv3891958copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,297-135,378,918 , GRCh38.p12 chr10: 47,357-133,565,414 TUBB8, PPP2R2D, 2085 more genes
    nsv3891568copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,379,241-93,219,169 , GRCh38.p12 chr10: 81,619,485-91,459,412 NAPGP1, IFIT3, 157 more genes
    nsv3891157copy number variation1nstd102humanPathogenic GRCh37 chr10: 98,087-135,477,883 , GRCh38.p12 chr10: 52,147-133,740,558 AGAP14P, LOC100505502, 2097 more genes
    nsv3891070copy number variation1nstd102humanPathogenic GRCh37 chr10: 69,040,366-93,194,993 , GRCh38.p12 chr10: 67,280,608-91,435,236 NRG3-AS1, FAM32CP, 441 more genes
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