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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6997857copy number variation1nstd229human GRCh38 chr17: 41,734,701-41,749,474 , GRCh37.p13 chr17|NW_003571052.1: 21,343-36,116 , GRCh37.p13 chr17: 39,890,953-39,905,726 HAP1
    nsv6989026copy number variation1nstd229human GRCh38 chr17: 41,717,421-41,727,245 , GRCh37.p13 chr17: 39,873,673-39,883,497 , GRCh37.p13 chr17|NW_003571052.1: 4,063-13,887 RNA5SP442, HAP1
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6250795mobile element insertion1nstd215human GRCh38 chr17: 41,716,909-41,716,909 , GRCh37.p13 chr17|NW_003571052.1: 3,551-3,551 , GRCh37.p13 chr17: 39,873,161-39,873,161 RNA5SP442, HAP1
    nsv6133061copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,890,001 , GRCh38.p12 chr17: 41,713,748-42,737,983 ACLY, ATP6V0A1, 51 more genes
    nsv6133060copy number variation1nstd213human GRCh37 chr17: 39,870,000-40,880,001 , GRCh38.p12 chr17: 41,713,748-42,727,983 ACLY, ATP6V0A1, 51 more genes
    nsv6089349insertion1nstd212human GRCh38 chr17: 41,730,030-41,730,030 , GRCh37.p13 chr17|NW_003571052.1: 16,672-16,672 , GRCh37.p13 chr17: 39,886,282-39,886,282 RN7SL399P, HAP1
    nsv6083446insertion1nstd212human GRCh38 chr17: 41,730,109-41,730,109 , GRCh37.p13 chr17|NW_003571052.1: 16,751-16,751 , GRCh37.p13 chr17: 39,886,361-39,886,361 HAP1, RN7SL399P
    nsv5976997insertion1nstd209human GRCh38 chr17: 41,716,896-41,716,896 , GRCh37.p13 chr17|NW_003571052.1: 3,538-3,538 , GRCh37.p13 chr17: 39,873,148-39,873,148 HAP1, RNA5SP442
    nsv5974388insertion1nstd209human GRCh38 chr17: 41,730,127-41,730,127 , GRCh37.p13 chr17|NW_003571052.1: 16,769-16,769 , GRCh37.p13 chr17: 39,886,379-39,886,379 HAP1, RN7SL399P
    nsv5720891mobile element insertion1nstd211human GRCh38 chr17: 41,729,579-41,729,579 , GRCh37.p13 chr17|NW_003571052.1: 16,221-16,221 , GRCh37.p13 chr17: 39,885,831-39,885,831 HAP1, RN7SL399P
    nsv5704745mobile element insertion2nstd211human GRCh38 chr17: 41,716,909-41,716,909 , GRCh37.p13 chr17|NW_003571052.1: 3,551-3,551 , GRCh37.p13 chr17: 39,873,161-39,873,161 RNA5SP442, HAP1
    nsv5653391insertion1nstd207human GRCh38 chr17: 41,730,084-41,730,084 , GRCh37.p13 chr17|NW_003571052.1: 16,726-16,726 , GRCh37.p13 chr17: 39,886,336-39,886,336 RN7SL399P, HAP1
    nsv5648184insertion1nstd207human GRCh38 chr17: 41,730,109-41,730,109 , GRCh37.p13 chr17|NW_003571052.1: 16,751-16,751 , GRCh37.p13 chr17: 39,886,361-39,886,361 HAP1, RN7SL399P
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5528612copy number variation1nstd206human GRCh38 chr17: 41,733,331-41,733,387 , GRCh37.p13 chr17: 39,889,583-39,889,639 , GRCh37.p13 chr17|NW_003571052.1: 19,973-20,029 HAP1
    nsv5420884mobile element insertion1nstd206human GRCh38 chr17: 41,716,909-41,716,925 , GRCh37.p13 chr17: 39,873,161-39,873,177 , GRCh37.p13 chr17|NW_003571052.1: 3,551-3,567 RNA5SP442, HAP1
    nsv5199460mobile element insertion1nstd203human GRCh38 chr17: 41,729,343-41,729,387 , GRCh37.p13 chr17|NW_003571052.1: 15,985-16,029 , GRCh37.p13 chr17: 39,885,595-39,885,639 HAP1, RN7SL399P
    nsv5189656mobile element insertion1nstd203human GRCh38 chr17: 41,729,549-41,729,549 , GRCh37.p13 chr17|NW_003571052.1: 16,191-16,191 , GRCh37.p13 chr17: 39,885,801-39,885,801 HAP1, RN7SL399P
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