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Items: 1 to 20 of 31

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4675165copy number variation1nstd102humanLikely benign GRCh37 chr8: 75,794,026-76,249,324 , GRCh38.p12 chr8: 74,881,791-75,337,089 CRISPLD1, CASC9, 2 more genes
    nsv3922848copy number variation1nstd102humanPathogenic NCBI36 chr8: 74,954,174-86,710,947 , GRCh37 chr8: 74,791,620-86,523,695 , GRCh38 chr8: 73,879,385-85,611,466 CRISPLD1, MITA1, 139 more genes
    nsv6315163copy number variation1nstd102humanPathogenic GRCh37 chr8: 75,904,944-87,097,083 , GRCh38.p12 chr8: 74,992,709-86,084,854 CRISPLD1, ZNF704, 137 more genes
    nsv3915614copy number variation1nstd102humanPathogenic GRCh37 chr8: 74,431,535-83,567,817 , NCBI36 chr8: 74,594,089-83,730,372 , GRCh38 chr8: 73,519,300-82,655,582 CRISPLD1, DSTNP3, 116 more genes
    nsv3895973copy number variation1nstd102humanPathogenic GRCh37 chr8: 75,197,438-81,685,526 , GRCh38.p12 chr8: 74,285,203-80,773,291 CRISPLD1, MIR2052, 72 more genes
    nsv3918656copy number variation1nstd102humanPathogenic GRCh37 chr8: 75,817,543-82,252,186 , NCBI36 chr8: 75,980,098-82,414,741 , GRCh38 chr8: 74,905,308-81,339,951 CRISPLD1, ZFHX4, 71 more genes
    nsv3890890copy number variation1nstd102humanPathogenic GRCh37 chr8: 74,942,333-80,413,867 , GRCh38.p12 chr8: 74,030,098-79,501,632 CRISPLD1, ZC2HC1A, 46 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 CRISPLD1, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 CRISPLD1, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 CRISPLD1, 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 CRISPLD1, RPL5P22, 2105 more genes
    nsv3898123copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385 CRISPLD1, SPAG1, 2105 more genes
    nsv3908608copy number variation1nstd102humanPathogenic GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028 CRISPLD1, LINC01617, 2105 more genes
    nsv3893757copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442 CRISPLD1, 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 CRISPLD1, 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 CRISPLD1, 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 CRISPLD1, 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 CRISPLD1, LOC112268023, 2103 more genes
    nsv3906425copy number variation1nstd102humanPathogenic GRCh37 chr8: 12,490,999-146,295,771 , GRCh38.p12 chr8: 12,633,490-145,070,385 CRISPLD1, 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 CRISPLD1, LOC105375693, 1718 more genes
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