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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139268copy number variation1nstd232human GRCh37.p13 chr17: 80,354,125-80,354,222 , GRCh38.p12 chr17: 82,396,249-82,396,346 OGFOD3
    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
    nsv7095424copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,332,201-80,758,892 , GRCh38.p12 chr17: 82,374,325-82,801,016 CYBC1, TRX-CAT1-8, 15 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
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6997283copy number variation1nstd229human GRCh38 chr17: 82,398,247-82,401,373 , GRCh37.p13 chr17: 80,356,123-80,359,249 OGFOD3
    nsv6990622copy number variation1nstd229human GRCh38 chr17: 82,384,920-82,394,196 , GRCh37.p13 chr17: 80,342,796-80,352,072 OGFOD3
    nsv6985420copy number variation1nstd229human GRCh38 chr17: 82,392,401-82,397,400 , GRCh37.p13 chr17: 80,350,277-80,355,276 OGFOD3
    nsv6984602copy number variation1nstd229human GRCh38 chr17: 82,382,146-82,394,711 , GRCh37.p13 chr17: 80,340,022-80,352,587 OGFOD3
    nsv6982690copy number variation1nstd229human GRCh38 chr17: 82,413,221-82,419,416 , GRCh37.p13 chr17: 80,371,097-80,377,292 OGFOD3, HEXD
    nsv6982221copy number variation1nstd229human GRCh38 chr17: 82,412,465-82,426,536 , GRCh37.p13 chr17: 80,370,341-80,384,412 HEXD, OGFOD3
    nsv6980167copy number variation1nstd229human GRCh38 chr17: 82,391,986-82,392,067 , GRCh37.p13 chr17: 80,349,862-80,349,943 OGFOD3
    nsv6980162copy number variation1nstd229human GRCh38 chr17: 82,276,139-82,416,061 , GRCh37.p13 chr17: 80,234,015-80,373,937 CD7, OGFOD3, 4 more genes
    nsv6624531copy number variation1nstd224human GRCh37 chr17: 80,339,729-80,384,338 , GRCh38.p12 chr17: 82,381,853-82,426,462 HEXD, OGFOD3
    nsv6624530copy number variation1nstd224human GRCh37 chr17: 80,235,063-80,374,899 , GRCh38.p12 chr17: 82,277,187-82,417,023 CD7, UTS2R, 5 more genes
    nsv6624323copy number variation1nstd224human GRCh37 chr17: 80,274,603-80,464,614 , GRCh38.p12 chr17: 82,316,727-82,506,738 SECTM1, HEXD, 8 more genes
    nsv6624127copy number variation1nstd224human GRCh37 chr17: 80,280,865-80,464,614 , GRCh38.p12 chr17: 82,322,989-82,506,738 UTS2R, SECTM1, 7 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
    nsv6533313copy number variation1nstd223human GRCh38 chr17: 82,294,456-82,671,315 , GRCh37.p13 chr17: 80,252,332-80,629,191 CD7, MIR4525, 14 more genes
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