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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6637224copy number variation1nstd102humanPathogenic GRCh37 chr8: 112,234,557-133,668,379 , GRCh38.p12 chr8: 111,222,328-132,656,133 ANXA13, RNU4-37P, 220 more genes
    nsv3876297copy number variation1nstd102humanPathogenic GRCh37 chr8: 114,508,086-129,040,004 , GRCh38.p12 chr8: 113,495,857-128,027,758 ANXA13, ZHX1-C8orf76, 172 more genes
    nsv3914003copy number variation1nstd102humanPathogenic NCBI36 chr8: 114,369,859-127,797,514 , GRCh38 chr8: 113,288,454-126,716,087 , GRCh37 chr8: 114,300,683-127,728,332 ANXA13, RNU6-442P, 154 more genes
    nsv4455511copy number variation1nstd102humanPathogenic GRCh37 chr8: 124,120,772-135,265,846 , GRCh38.p12 chr8: 123,108,532-134,253,603 ANXA13, MTSS1, 148 more genes
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 ANXA13, LINC02964, 115 more genes
    nsv4457220copy number variation1nstd102humanPathogenic GRCh37 chr8: 123,074,293-131,113,892 , GRCh38.p12 chr8: 122,062,054-130,101,646 ANXA13, ZHX1-C8orf76, 117 more genes
    nsv3915173copy number variation1nstd102humanPathogenic NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636 ANXA13, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 ANXA13, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 ANXA13, LOC101929488, 2105 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 ANXA13, RPL5P22, 2105 more genes
    nsv3898123copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385 ANXA13, SPAG1, 2105 more genes
    nsv3908608copy number variation1nstd102humanPathogenic GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028 ANXA13, LINC01617, 2105 more genes
    nsv3893757copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442 ANXA13, LOC105375890, 2105 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 ANXA13, LOC112268023, 2105 more genes
    nsv3914307copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,605-146,280,167 , GRCh38 chr8: 241,605-145,054,781 , NCBI36 chr8: 181,605-146,250,971 ANXA13, LOC107986897, 2104 more genes
    nsv3919282copy number variation1nstd102humanPathogenic GRCh37 chr8: 191,530-146,280,020 , GRCh38 chr8: 241,530-145,054,634 , NCBI36 chr8: 181,530-146,250,824 ANXA13, MIR4662B, 2104 more genes
    nsv3919200copy number variation1nstd102humanPathogenic GRCh38 chr8: 241,530-145,049,449 , GRCh37 chr8: 191,530-146,274,835 , NCBI36 chr8: 181,530-146,245,639 ANXA13, LOC112268023, 2103 more genes
    nsv3906425copy number variation1nstd102humanPathogenic GRCh37 chr8: 12,490,999-146,295,771 , GRCh38.p12 chr8: 12,633,490-145,070,385 ANXA13, LOC112268016, 1819 more genes
    nsv3915762copy number variation1nstd102humanPathogenic NCBI36 chr8: 21,193,313-146,266,575 , GRCh38 chr8: 21,291,522-145,070,385 , GRCh37 chr8: 21,149,033-146,295,771 ANXA13, LOC105375693, 1718 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 ANXA13, TERF1, 1511 more genes
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