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Items: 1 to 20 of 68

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098167copy number variation1nstd102humanPathogenic GRCh37 chr8: 145,137,634-145,138,963 , GRCh38.p12 chr8: 144,082,731-144,084,060 GPAA1
    nsv4675029copy number variation1nstd102humanPathogenic GRCh37 chr8: 142,132,678-145,569,441 , GRCh38.p12 chr8: 141,122,579-144,345,779 GPAA1, RHPN1-AS1, 117 more genes
    nsv3911442copy number variation1nstd102humanPathogenic NCBI36 chr8: 142,823,655-145,267,498 , GRCh37 chr8: 142,764,538-145,195,510 , GRCh38 chr8: 141,738,068-144,140,607 GPAA1, GRINA, 94 more genes
    nsv6312709copy number variation2nstd102humanPathogenic GRCh37 chr8: 144,295,143-145,701,139 , GRCh38.p12 chr8: 143,213,268-144,475,756 GPAA1, MIR10400, 83 more genes
    nsv3924581copy number variation1nstd102humanPathogenic NCBI36 chr8: 144,838,977-145,482,487 , GRCh37 chr8: 144,940,777-145,511,679 , GRCh38 chr8: 143,684,819-144,287,978 GPAA1, SCX, 35 more genes
    nsv4349929copy number variation1nstd102humanPathogenic GRCh37 chr8: 144,879,444-145,199,846 , GRCh38.p12 chr8: 143,797,274-144,144,943 GPAA1, TSSK5P, 22 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 GPAA1, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 GPAA1, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 GPAA1, 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 GPAA1, RPL5P22, 2105 more genes
    nsv3898123copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385 GPAA1, SPAG1, 2105 more genes
    nsv3908608copy number variation1nstd102humanPathogenic GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028 GPAA1, LINC01617, 2105 more genes
    nsv3893757copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442 GPAA1, 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 GPAA1, 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 GPAA1, 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 GPAA1, 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 GPAA1, LOC112268023, 2103 more genes
    nsv3906425copy number variation1nstd102humanPathogenic GRCh37 chr8: 12,490,999-146,295,771 , GRCh38.p12 chr8: 12,633,490-145,070,385 GPAA1, 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 GPAA1, LOC105375693, 1718 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 GPAA1, TERF1, 1511 more genes
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