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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5531475copy number variation1nstd206human GRCh38 chr17: 61,482,671-61,482,725 , GRCh37.p13 chr17: 59,560,032-59,560,086 TBX4
    nsv5361564translocation1nstd200human GRCh38 chr17: 61,474,354-61,474,354 , GRCh38 chr17: 61,474,268-61,474,268 , GRCh37.p13 chr17: 59,551,629-59,551,629 , GRCh37.p13 chr17: 59,551,715-59,551,715 TBX4
    nsv5361563translocation1nstd200human GRCh38 chr17: 61,458,199-61,458,199 , GRCh38 chr17: 61,458,141-61,458,141 , GRCh37.p13 chr17: 59,535,502-59,535,502 , GRCh37.p13 chr17: 59,535,560-59,535,560 TBX4
    nsv5329113copy number variation1nstd204human GRCh38.p13 chr17: 61,447,086-61,453,032 , GRCh37.p13 chr17: 59,524,447-59,530,393 TBX4
    nsv5290260copy number variation1nstd204human GRCh38.p13 chr17: 61,446,823-61,453,297 , GRCh37.p13 chr17: 59,524,184-59,530,658 TBX4
    nsv5284287copy number variation1nstd204human GRCh38.p13 chr17: 61,447,101-61,453,000 , GRCh37.p13 chr17: 59,524,462-59,530,361 TBX4
    nsv5010504copy number variation1nstd200human GRCh38 chr17: 61,476,454-61,478,583 , GRCh37.p13 chr17: 59,553,815-59,555,944 TBX4
    nsv5010503copy number variation1nstd200human GRCh38 chr17: 61,469,664-61,471,154 , GRCh37.p13 chr17: 59,547,025-59,548,515 TBX4
    nsv5010502copy number variation1nstd200human GRCh38 chr17: 61,449,246-61,451,409 , GRCh37.p13 chr17: 59,526,607-59,528,770 TBX4
    nsv5010501copy number variation1nstd200human GRCh38 chr17: 61,447,092-61,453,029 , GRCh37.p13 chr17: 59,524,453-59,530,390 TBX4
    nsv4851570copy number variation1nstd200human GRCh37 chr17: 59,526,607-59,528,770 , GRCh38.p12 chr17: 61,449,246-61,451,409 TBX4
    nsv4851569copy number variation1nstd200human GRCh37 chr17: 59,524,453-59,530,390 , GRCh38.p12 chr17: 61,447,092-61,453,029 TBX4
    nsv4457799copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302 PECAM1, TBX2-AS1, 215 more genes
    nsv4432562copy number variation1nstd172human GRCh37.p13 chr17: 59,560,922-59,561,950 , GRCh38.p12 chr17: 61,483,561-61,484,589 TBX4
    nsv4349383copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,357,088-66,306,668 , GRCh38.p12 chr17: 59,279,727-68,310,527 FAM136DP, HELZ, 214 more genes
    nsv4349356copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 58,121,190-60,140,614 , GRCh38.p12 chr17: 60,043,829-62,063,253 CA4, TBX2, 39 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4271308copy number variation1nstd166human GRCh37.p13 chr17: 59,553,815-59,555,944 , GRCh38.p12 chr17: 61,476,454-61,478,583 TBX4
    nsv3918670copy number variation1nstd102humanPathogenic GRCh37 chr17: 58,172,700-60,315,303 , GRCh38 chr17: 60,095,339-62,237,942 , NCBI36 chr17: 55,527,482-57,670,085 MED13, RPL36AP46, 37 more genes
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