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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098190copy number variation1nstd102humanUncertain significance GRCh37 chr8: 98,358,247-106,815,766 , GRCh38.p12 chr8: 97,346,019-105,803,538 RNU6-914P, RPL30, 159 more genes
    nsv7077334inversion1nstd229human GRCh38 chr8: 102,796,562-104,427,483 , GRCh37.p13 chr8: 103,808,790-105,439,711 DCSTAMP, LOC107984007, 33 more genes
    nsv7076737inversion1nstd229human GRCh38 chr8: 103,194,182-103,198,172 , GRCh37.p13 chr8: 104,206,410-104,210,400 BAALC
    nsv7075711inversion1nstd229human GRCh38 chr8: 102,102,164-111,409,427 , GRCh37.p13 chr8: 103,114,392-112,421,656 LINC01181, LOC105375690, 118 more genes
    nsv7073376inversion1nstd229human GRCh38 chr8: 99,051,852-103,793,725 , GRCh37.p13 chr8: 100,064,080-104,805,953 RNU4-83P, RN7SL563P, 102 more genes
    nsv7072980inversion1nstd229human GRCh38 chr8: 102,790,775-104,428,155 , GRCh37.p13 chr8: 103,803,003-105,440,383 DCSTAMP, ATP6V1C1, 33 more genes
    nsv7071528inversion1nstd229human GRCh38 chr8: 103,103,016-104,690,333 , GRCh37.p13 chr8: 104,115,244-105,702,561 LOC105375690, DCAF13, 27 more genes
    nsv6858085copy number variation1nstd229human GRCh38 chr8: 103,174,080-103,349,054 , GRCh37.p13 chr8: 104,186,308-104,361,282 SNORD173, FZD6, 2 more genes
    nsv6857832copy number variation1nstd229human GRCh38 chr8: 103,210,654-103,293,600 , GRCh37.p13 chr8: 104,222,882-104,305,828 LOC105369147, BAALC
    nsv6857508copy number variation1nstd229human GRCh38 chr8: 103,113,405-103,222,339 , GRCh37.p13 chr8: 104,125,633-104,234,567 BAALC, BAALC-AS2, 3 more genes
    nsv6851448copy number variation1nstd229human GRCh38 chr8: 103,071,801-103,331,000 , GRCh37.p13 chr8: 104,084,029-104,343,228 MTND1P5, BAALC-AS1, 11 more genes
    nsv6845547copy number variation1nstd229human GRCh38 chr8: 103,189,601-103,384,200 , GRCh37.p13 chr8: 104,201,829-104,396,428 SNORD173, CTHRC1, 4 more genes
    nsv6843413copy number variation1nstd229human GRCh38 chr8: 103,121,501-103,140,237 , GRCh37.p13 chr8: 104,133,729-104,152,465 LINC01181, BAALC-AS2, 1 more genes
    nsv6841777copy number variation1nstd229human GRCh38 chr8: 103,171,078-103,179,325 , GRCh37.p13 chr8: 104,183,306-104,191,553 BAALC, BAALC-AS1
    nsv6838178copy number variation1nstd229human GRCh38 chr8: 103,189,644-103,200,317 , GRCh37.p13 chr8: 104,201,872-104,212,545 BAALC
    nsv6636450copy number variation1nstd102humanPathogenic GRCh37 chr8: 79,409,349-119,040,631 , GRCh38.p12 chr8: 78,497,114-118,028,392 MIR2053, RPS2P33, 507 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6569911inversion1nstd223human GRCh38 chr8: 103,191,115-103,192,076 , GRCh37.p13 chr8: 104,203,343-104,204,304 BAALC
    nsv6429630copy number variation1nstd223human GRCh38 chr8: 103,175,036-103,175,626 , GRCh37.p13 chr8: 104,187,264-104,187,854 BAALC
    nsv6422997copy number variation1nstd223human GRCh38 chr8: 103,187,857-103,188,656 , GRCh37.p13 chr8: 104,200,085-104,200,884 BAALC
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