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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6997795copy number variation1nstd229human GRCh38 chr17: 64,523,424-64,527,387 , GRCh37.p13 chr17|NW_003315947.1: 327,271-331,234 , GRCh37.p13 chr17: 62,519,542-62,523,505 CEP95
    nsv6997739copy number variation1nstd229human GRCh38 chr17: 64,511,763-64,513,428 , GRCh37.p13 chr17|NW_003315947.1: 315,610-317,275 , GRCh37.p13 chr17: 62,507,881-62,509,546 CEP95
    nsv6993966copy number variation1nstd229human GRCh38 chr17: 64,514,130-64,529,595 , GRCh37.p13 chr17|NW_003315947.1: 317,977-333,442 , GRCh37.p13 chr17: 62,510,248-62,525,713 CEP95
    nsv6993407copy number variation1nstd229human GRCh38 chr17: 64,524,172-64,528,430 , GRCh37.p13 chr17|NW_003315947.1: 328,019-332,277 , GRCh37.p13 chr17: 62,520,290-62,524,548 CEP95
    nsv6991550copy number variation1nstd229human GRCh38 chr17: 64,536,751-64,552,262 , GRCh37.p13 chr17|NW_003315947.1: 340,598-356,109 , GRCh37.p13 chr17: 62,532,869-62,548,380 SMURF2, CEP95
    nsv6986145copy number variation1nstd229human GRCh38 chr17: 64,535,727-64,539,548 , GRCh37.p13 chr17|NW_003315947.1: 339,574-343,395 , GRCh37.p13 chr17: 62,531,845-62,535,666 CEP95
    nsv6591666inversion1nstd223human GRCh38 chr17: 64,530,106-64,530,571 , GRCh37.p13 chr17: 62,526,224-62,526,689 , GRCh37.p13 chr17|NW_003315947.1: 333,953-334,418 CEP95
    nsv6586910inversion1nstd223human GRCh38 chr17: 64,509,633-64,510,741 , GRCh37.p13 chr17|NW_003315947.1: 313,480-314,588 , GRCh37.p13 chr17: 62,505,751-62,506,859 CEP95
    nsv6530811copy number variation1nstd223human GRCh38 chr17: 64,529,201-64,531,300 , GRCh37.p13 chr17: 62,525,319-62,527,418 , GRCh37.p13 chr17|NW_003315947.1: 333,048-335,147 CEP95
    nsv6530228copy number variation1nstd223human GRCh38 chr17: 64,397,624-65,005,750 , GRCh37.p13 chr17: 62,649,313-63,001,868 LOC105371860, PECAM1, 25 more genes
    nsv6526282copy number variation1nstd223human GRCh38 chr17: 64,524,172-64,528,426 , GRCh37.p13 chr17: 62,520,290-62,524,544 , GRCh37.p13 chr17|NW_003315947.1: 328,019-332,273 CEP95
    nsv6517239copy number variation1nstd223human GRCh38 chr17: 64,520,837-64,527,914 , GRCh37.p13 chr17|NW_003315947.1: 324,684-331,761 , GRCh37.p13 chr17: 62,516,955-62,524,032 CEP95
    nsv6203406copy number variation1nstd214human GRCh38 chr17: 64,527,857-64,527,908 , GRCh37.p13 chr17|NW_003315947.1: 331,704-331,755 , GRCh37.p13 chr17: 62,523,975-62,524,026 CEP95
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5520511copy number variation1nstd206human GRCh38 chr17: 64,526,861-64,526,920 , GRCh37.p13 chr17: 62,522,979-62,523,038 , GRCh37.p13 chr17|NW_003315947.1: 330,708-330,767 CEP95
    nsv5145817mobile element insertion1nstd203human GRCh38 chr17: 64,524,239-64,524,256 , GRCh37.p13 chr17|NW_003315947.1: 328,086-328,103 , GRCh37.p13 chr17: 62,520,357-62,520,374 CEP95
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5010625copy number variation1nstd200human GRCh38 chr17: 64,536,414-64,536,512 , GRCh37.p13 chr17|NW_003315947.1: 340,261-340,359 , GRCh37.p13 chr17: 62,532,532-62,532,630 CEP95
    nsv5010624copy number variation1nstd200human GRCh38 chr17: 64,524,172-64,528,426 , GRCh37.p13 chr17|NW_003315947.1: 328,019-332,273 , GRCh37.p13 chr17: 62,520,290-62,524,544 CEP95
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