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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143890copy number variation1nstd232human GRCh37.p13 chr17: 80,182,019-80,182,154 , GRCh38.p12 chr17: 82,224,143-82,224,278 SLC16A3
    nsv7140193copy number variation1nstd232human GRCh37.p13 chr17: 80,185,510-80,185,560 , GRCh38.p12 chr17: 82,227,634-82,227,684 SLC16A3
    nsv7098933copy number variation1nstd102humanUncertain significance GRCh38 chr17: 82,004,063-83,087,346 , GRCh37.p13 chr17: 79,961,939-81,045,222 ZNF750, LINC01970, 37 more genes
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7094997copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,891,090-80,333,370 , GRCh38.p12 chr17: 81,933,214-82,375,494 LOC105371939, LINC01970, 22 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6994627copy number variation1nstd229human GRCh38 chr17: 82,231,401-82,240,500 , GRCh37.p13 chr17: 80,189,277-80,198,376 CSNK1D, MIR6787, 1 more genes
    nsv6988806copy number variation1nstd229human GRCh38 chr17: 82,225,601-82,241,900 , GRCh37.p13 chr17: 80,183,477-80,199,776 CSNK1D, MIR6787, 1 more genes
    nsv6985160copy number variation1nstd229human GRCh38 chr17: 82,233,801-82,239,200 , GRCh37.p13 chr17: 80,191,677-80,197,076 MIR6787, CSNK1D, 1 more genes
    nsv6983934copy number variation1nstd229human GRCh38 chr17: 82,219,001-82,224,600 , GRCh37.p13 chr17: 80,176,877-80,182,476 SLC16A3
    nsv6983653copy number variation1nstd229human GRCh38 chr17: 82,239,901-82,241,900 , GRCh37.p13 chr17: 80,197,777-80,199,776 SLC16A3, CSNK1D
    nsv6982912copy number variation1nstd229human GRCh38 chr17: 82,213,174-82,218,587 , GRCh37.p13 chr17: 80,171,050-80,176,463 CCDC57, SLC16A3
    nsv6979045copy number variation1nstd229human GRCh38 chr17: 82,161,356-82,218,840 , GRCh37.p13 chr17: 80,119,232-80,176,716 CCDC57, SLC16A3
    nsv6978850copy number variation1nstd229human GRCh38 chr17: 82,212,601-82,284,300 , GRCh37.p13 chr17: 80,170,477-80,242,176 SLC16A3, CCDC57, 2 more genes
    nsv6533522copy number variation1nstd223human GRCh38 chr17: 82,052,201-82,542,400 , GRCh37.p13 chr17: 80,010,077-80,500,276 MIR6787, CD7, 19 more genes
    nsv6530547copy number variation1nstd223human GRCh38 chr17: 82,234,326-82,235,418 , GRCh37.p13 chr17: 80,192,202-80,193,294 SLC16A3, MIR6787
    nsv6526516copy number variation1nstd223human GRCh38 chr17: 82,225,801-82,226,400 , GRCh37.p13 chr17: 80,183,677-80,184,276 SLC16A3
    nsv6525507copy number variation1nstd223human GRCh38 chr17: 81,799,201-82,693,800 , GRCh37.p13 chr17: 79,759,050-80,651,676 CENPX, RFNG, 47 more genes
    nsv6518969copy number variation1nstd223human GRCh38 chr17: 82,181,801-82,461,700 , GRCh37.p13 chr17: 80,139,677-80,419,576 LINC01970, NARF, 12 more genes
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