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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943515copy number variation1nstd209human GRCh38 chr16: 75,487,442-75,488,240 , GRCh37.p13 chr16: 75,521,340-75,522,138 CHST6
    nsv5882874copy number variation1nstd209human GRCh38 chr16: 75,464,053-75,484,146 , GRCh37.p13 chr16: 75,497,951-75,518,044 TMEM170A, CHST6
    nsv5881322copy number variation2nstd209human GRCh38 chr16: 75,488,433-75,490,119 , GRCh37.p13 chr16: 75,522,331-75,524,017 CHST6
    nsv5874789copy number variation1nstd209human GRCh38 chr16: 75,468,479-75,471,078 , GRCh37.p13 chr16: 75,502,377-75,504,976 CHST6
    nsv5871226copy number variation1nstd209human GRCh38 chr16: 75,489,620-75,508,325 , GRCh37.p13 chr16: 75,523,518-75,542,223 CHST6, TMEM231P1
    nsv5869229copy number variation1nstd209human GRCh38 chr16: 75,490,720-75,503,452 , GRCh37.p13 chr16: 75,524,618-75,537,350 CHST6, TMEM231P1
    nsv5868146copy number variation1nstd209human GRCh38 chr16: 75,484,947-75,489,919 , GRCh37.p13 chr16: 75,518,845-75,523,817 CHST6
    nsv5551279insertion1nstd206human GRCh38 chr16: 75,491,182-75,491,191 , GRCh37.p13 chr16: 75,525,080-75,525,089 CHST6
    nsv5519783copy number variation1nstd206human GRCh38 chr16: 75,462,682-75,516,682 , GRCh37.p13 chr16: 75,496,580-75,550,580 TMEM170A, TMEM231P1, 1 more genes
    nsv5517394copy number variation1nstd206human GRCh38 chr16: 75,488,773-75,490,295 , GRCh37.p13 chr16: 75,522,671-75,524,193 CHST6
    nsv5516412copy number variation1nstd206human GRCh38 chr16: 75,476,853-75,493,999 , GRCh37.p13 chr16: 75,510,751-75,527,897 CHST6
    nsv5365711translocation1nstd200human GRCh38 chr16: 75,488,774-75,488,774 , GRCh38 chr16: 75,490,207-75,490,207 , GRCh37.p13 chr16: 75,524,105-75,524,105 , GRCh37.p13 chr16: 75,522,672-75,522,672 CHST6
    nsv5365710translocation1nstd200human GRCh38 chr16: 75,530,062-75,530,062 , GRCh38 chr16: 75,479,687-75,479,687 , GRCh37.p13 chr16: 75,563,960-75,563,960 , GRCh37.p13 chr16: 75,513,585-75,513,585 CHST5, CHST6
    nsv5318329copy number variation1nstd204human GRCh37.p13 chr16: 75,486,130-75,510,031 , GRCh38.p13 chr16: 75,452,232-75,476,133 CHST6, TMEM170A
    nsv5210083mobile element deletion1nstd204human GRCh38.p13 chr16: 75,476,262-75,476,594 , GRCh37.p13 chr16: 75,510,160-75,510,492 CHST6
    nsv5141478mobile element insertion1nstd203human GRCh38 chr16: 75,484,209-75,484,242 , GRCh37.p13 chr16: 75,518,107-75,518,140 CHST6
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5005869copy number variation1nstd200human GRCh38 chr16: 75,487,302-75,502,700 , GRCh37.p13 chr16: 75,521,200-75,536,598 TMEM231P1, CHST6
    nsv5005867copy number variation1nstd200human GRCh38 chr16: 75,460,894-75,508,740 , GRCh37.p13 chr16: 75,494,792-75,542,638 TMEM231P1, TMEM170A, 1 more genes
    nsv5005866copy number variation1nstd200human GRCh38 chr16: 75,456,497-75,508,609 , GRCh37.p13 chr16: 75,490,395-75,542,507 CHST6, TMEM170A, 1 more genes
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