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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943874copy number variation1nstd209human GRCh38 chr16: 75,440,603-75,449,609 , GRCh37.p13 chr16: 75,474,501-75,483,507 TMEM170A
    nsv5939987copy number variation1nstd209human GRCh38 chr16: 75,454,151-75,454,237 , GRCh37.p13 chr16: 75,488,049-75,488,135 TMEM170A
    nsv5931812copy number variation1nstd209human GRCh38 chr16: 74,874,044-75,453,217 , GRCh37.p13 chr16: 74,907,942-75,487,115 , ZNRF1, 12 more genes
    nsv5929121copy number variation1nstd209human GRCh38 chr16: 75,457,083-75,457,212 , GRCh37.p13 chr16: 75,490,981-75,491,110 TMEM170A
    nsv5882874copy number variation1nstd209human GRCh38 chr16: 75,464,053-75,484,146 , GRCh37.p13 chr16: 75,497,951-75,518,044 TMEM170A, CHST6
    nsv5870146copy number variation1nstd209human GRCh38 chr16: 75,453,323-75,461,876 , GRCh37.p13 chr16: 75,487,221-75,495,774 TMEM170A
    nsv5869677copy number variation1nstd209human GRCh38 chr16: 75,440,443-75,449,554 , GRCh37.p13 chr16: 75,474,341-75,483,452 TMEM170A
    nsv5711636mobile element insertion1nstd211human GRCh38 chr16: 75,463,298-75,463,298 , GRCh37.p13 chr16: 75,497,196-75,497,196 TMEM170A
    nsv5595874copy number variation1nstd207human GRCh38 chr16: 75,454,151-75,454,237 , GRCh37.p13 chr16: 75,488,049-75,488,135 TMEM170A
    nsv5586959copy number variation1nstd207human GRCh38 chr16: 75,457,083-75,457,212 , GRCh37.p13 chr16: 75,490,981-75,491,110 TMEM170A
    nsv5525061copy number variation1nstd206human GRCh38 chr16: 75,454,154-75,454,238 , GRCh37.p13 chr16: 75,488,052-75,488,136 TMEM170A
    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
    nsv5514817copy number variation1nstd206human GRCh38 chr16: 75,459,828-75,468,918 , GRCh37.p13 chr16: 75,493,726-75,502,816 TMEM170A
    nsv5514398copy number variation1nstd206human GRCh38 chr16: 75,457,090-75,457,213 , GRCh37.p13 chr16: 75,490,988-75,491,111 TMEM170A
    nsv5421632mobile element insertion1nstd206human GRCh38 chr16: 75,463,298-75,463,349 , GRCh37.p13 chr16: 75,497,196-75,497,247 TMEM170A
    nsv5341659translocation1nstd200human GRCh37 chr16: 75,490,988-75,490,988 , GRCh37 chr16: 75,491,111-75,491,111 , GRCh38.p12 chr16: 75,457,213-75,457,213 , GRCh38.p12 chr16: 75,457,090-75,457,090 TMEM170A
    nsv5318329copy number variation1nstd204human GRCh37.p13 chr16: 75,486,130-75,510,031 , GRCh38.p13 chr16: 75,452,232-75,476,133 CHST6, TMEM170A
    nsv5297444copy number variation1nstd204human GRCh38.p13 chr16: 75,452,223-75,468,728 , GRCh37.p13 chr16: 75,486,121-75,502,626 TMEM170A
    nsv5286982copy number variation1nstd204human GRCh38.p13 chr16: 75,452,223-75,456,322 , GRCh37.p13 chr16: 75,486,121-75,490,220 TMEM170A
    nsv5144245mobile element insertion1nstd203human GRCh38 chr16: 75,448,180-75,448,199 , GRCh37.p13 chr16: 75,482,078-75,482,097 TMEM170A
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