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Items: 1 to 20 of 339

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7098901copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 21,925,038-26,372,195 , GRCh38.p12 chr8: 22,067,527-26,514,679 BMP1, POLR3D, 95 more genes
    nsv6857122copy number variation1nstd229human GRCh38 chr8: 22,640,543-22,651,328 , GRCh37.p13 chr8: 22,498,056-22,508,841 BIN3, BIN3-IT1
    nsv6855264copy number variation1nstd229human GRCh38 chr8: 22,620,380-22,621,074 , GRCh37.p13 chr8: 22,477,893-22,478,587 CCAR2, BIN3
    nsv6845836copy number variation1nstd229human GRCh38 chr8: 22,583,801-22,742,400 , GRCh37.p13 chr8: 22,441,314-22,599,913 PEBP4, LOC105379321, 10 more genes
    nsv6845054copy number variation1nstd229human GRCh38 chr8: 22,648,266-22,651,796 , GRCh37.p13 chr8: 22,505,779-22,509,309 BIN3
    nsv6843777copy number variation1nstd229human GRCh38 chr8: 22,659,601-22,663,800 , GRCh37.p13 chr8: 22,517,114-22,521,313 BIN3
    nsv6843747copy number variation1nstd229human GRCh38 chr8: 22,624,375-22,624,485 , GRCh37.p13 chr8: 22,481,888-22,481,998 BIN3
    nsv6843212copy number variation1nstd229human GRCh38 chr8: 22,643,249-22,643,455 , GRCh37.p13 chr8: 22,500,762-22,500,968 BIN3
    nsv6840924copy number variation1nstd229human GRCh38 chr8: 22,622,617-22,636,625 , GRCh37.p13 chr8: 22,480,130-22,494,138 BIN3
    nsv6839411copy number variation1nstd229human GRCh38 chr8: 22,644,601-22,652,000 , GRCh37.p13 chr8: 22,502,114-22,509,513 BIN3
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6431591copy number variation1nstd223human GRCh38 chr8: 22,648,262-22,651,792 , GRCh37.p13 chr8: 22,505,775-22,509,305 BIN3
    nsv6420333copy number variation1nstd223human GRCh38 chr8: 22,622,617-22,636,623 , GRCh37.p13 chr8: 22,480,130-22,494,136 BIN3
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 LOC101928016, RPL23AP54, 568 more genes
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6315176copy number variation1nstd102humanPathogenic GRCh37 chr8: 19,779,604-26,531,980 , GRCh38.p12 chr8: 19,922,093-26,674,463 TNFRSF10C, TNFRSF10A, 121 more genes
    nsv6312718copy number variation2nstd102humanUncertain significance GRCh37 chr8: 21,900,440-23,564,111 , GRCh38.p12 chr8: 22,042,929-23,706,598 LOC105379327, RPL23AP55, 56 more genes
    nsv6269415copy number variation1nstd214human GRCh38 chr8: 22,645,814-22,645,897 , GRCh37.p13 chr8: 22,503,327-22,503,410 BIN3
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