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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145734insertion1nstd232human GRCh37.p13 chr1: 91,985,840-91,985,840 , GRCh38.p12 chr1: 91,520,283-91,520,283 CDC7, LOC102723436
    nsv7145083copy number variation1nstd232human GRCh37.p13 chr1: 91,977,246-91,977,335 , GRCh38.p12 chr1: 91,511,689-91,511,778 CDC7
    nsv7138588insertion1nstd232human GRCh37.p13 chr1: 91,980,552-91,980,552 , GRCh38.p12 chr1: 91,514,995-91,514,995 CDC7
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv7050257inversion1nstd229human GRCh38 chr1: 90,043,458-91,855,366 , GRCh37.p13 chr1: 90,509,016-92,320,923 SNORD3G, LINC01763, 24 more genes
    nsv7043892inversion1nstd229human GRCh38 chr1: 90,652,907-91,933,179 , GRCh37.p13 chr1: 91,118,464-92,398,736 ZNF644, RPL5P6, 17 more genes
    nsv6657288copy number variation1nstd229human GRCh38 chr1: 91,506,101-91,512,700 , GRCh37.p13 chr1: 91,971,658-91,978,257 CDC7
    nsv6657148copy number variation1nstd229human GRCh38 chr1: 91,499,383-91,500,023 , GRCh37.p13 chr1: 91,964,940-91,965,580 CDC7
    nsv6657064copy number variation1nstd229human GRCh38 chr1: 91,159,650-91,619,553 , GRCh37.p13 chr1: 91,625,207-92,085,110 HFM1, LOC107985417, 6 more genes
    nsv6657058copy number variation1nstd229human GRCh38 chr1: 91,366,292-92,033,167 , GRCh37.p13 chr1: 91,831,849-92,498,724 LOC102723436, EPHX4, 10 more genes
    nsv6657055copy number variation1nstd229human GRCh38 chr1: 91,282,006-91,578,137 , GRCh37.p13 chr1: 91,747,563-92,043,694 FEN1P1, LOC102723436, 5 more genes
    nsv6626481copy number variation1nstd224human GRCh37 chr1: 91,967,385-91,989,979 , GRCh38.p12 chr1: 91,501,828-91,524,422 CDC7, LOC102723436
    nsv6542421inversion1nstd223human GRCh38 chr1: 85,951,963-92,104,665 , GRCh37.p13 chr1: 86,417,646-92,570,222 LOC105378844, LINC01773, 104 more genes
    nsv6334931copy number variation1nstd223human GRCh38 chr1: 91,515,733-91,520,729 , GRCh37.p13 chr1: 91,981,290-91,986,286 LOC102723436, CDC7
    nsv6334739copy number variation1nstd223human GRCh38 chr1: 91,095,691-93,048,861 , GRCh37.p13 chr1: 91,561,248-93,514,418 LOC107985417, BRDT, 38 more genes
    nsv6333934copy number variation1nstd223human GRCh38 chr1: 91,514,287-91,514,635 , GRCh37.p13 chr1: 91,979,844-91,980,192 CDC7
    nsv6333307copy number variation1nstd223human GRCh38 chr1: 91,338,070-91,815,598 , GRCh37.p13 chr1: 91,803,627-92,281,155 CDC7, WDR82P2, 7 more genes
    nsv6326156copy number variation1nstd223human GRCh38 chr1: 91,496,401-91,507,100 , GRCh37.p13 chr1: 91,961,958-91,972,657 LOC105378856, CDC7
    nsv6324434copy number variation1nstd223human GRCh38 chr1: 91,511,801-91,512,500 , GRCh37.p13 chr1: 91,977,358-91,978,057 CDC7
    nsv6320596copy number variation1nstd223human GRCh38 chr1: 91,491,401-91,573,200 , GRCh37.p13 chr1: 91,956,958-92,038,757 WDR82P2, CDC7, 2 more genes
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