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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925176copy number variation1nstd209human GRCh38 chr10: 102,736,166-102,736,286 , GRCh37.p13 chr10: 104,495,923-104,496,043 SFXN2
    nsv5508559copy number variation1nstd206human GRCh38 chr10: 102,733,295-102,736,615 , GRCh37.p13 chr10: 104,493,052-104,496,372 SFXN2
    nsv5505113copy number variation1nstd206human GRCh38 chr10: 102,736,166-102,736,287 , GRCh37.p13 chr10: 104,495,923-104,496,044 SFXN2
    nsv5317306copy number variation1nstd204human GRCh38.p13 chr10: 102,726,984-102,734,625 , GRCh37.p13 chr10: 104,486,741-104,494,382 SFXN2
    nsv5241285copy number variation1nstd204human GRCh38.p13 chr10: 102,727,058-102,734,871 , GRCh37.p13 chr10: 104,486,815-104,494,628 SFXN2
    nsv4847085copy number variation1nstd200human GRCh37 chr10: 104,486,751-104,494,373 , GRCh38.p12 chr10: 102,726,994-102,734,616 SFXN2
    nsv4679283copy number variation1nstd189human GRCh37.p13 chr10: 104,468,424-105,156,097 , GRCh38.p12 chr10: 102,708,667-103,396,340 , ARL3, 25 more genes
    nsv4578056mobile element insertion1nstd166human GRCh37.p13 chr10: 104,483,983-104,483,983 , GRCh38.p12 chr10: 102,724,226-102,724,226 SFXN2
    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
    nsv4187936copy number variation1nstd166human GRCh37.p13 chr10: 104,485,169-104,485,242 , GRCh38.p12 chr10: 102,725,412-102,725,485 SFXN2
    nsv4178300copy number variation1nstd166human GRCh37.p13 chr10: 104,500,500-104,506,500 , GRCh38.p12 chr10: 102,740,743-102,746,743 WBP1L, SFXN2
    nsv4178208copy number variation1nstd166human GRCh37.p13 chr10: 104,495,923-104,496,043 , GRCh38.p12 chr10: 102,736,166-102,736,286 SFXN2
    nsv4172894copy number variation1nstd166human GRCh37.p13 chr10: 104,499,463-104,499,821 , GRCh38.p12 chr10: 102,739,706-102,740,064 SFXN2
    nsv3966503insertion1nstd168human GRCh38 chr10: 102,691,761-102,715,440 , GRCh37.p13 chr10: 104,451,518-104,475,197 SFXN2, ARL3
    nsv3924696copy number variation1nstd102humanPathogenic GRCh38 chr10: 102,243,341-103,929,730 , GRCh37 chr10: 104,003,098-105,689,488 , NCBI36 chr10: 103,993,088-105,679,478 MIR146B, RPL23AP58, 48 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
    nsv3922274copy number variation1nstd102humanUncertain significance NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422 DPCD, LOC105378467, 504 more genes
    nsv3921919copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082 MIR4295, BORCS7, 508 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
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