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Items: 1 to 20 of 472

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6289975copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,257,445-88,409,236 , GRCh38.p12 chr16: 88,223,839-88,355,777 LOC107984862
    nsv6289940copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,285,490-88,362,122 , GRCh38.p12 chr16: 88,251,884-88,328,516 LOC107984862
    nsv4716437copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,809,347-89,883,065 , GRCh38.p12 chr16: 89,742,939-89,816,657 FANCA
    nsv7095121copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,815,049-89,883,033 , GRCh38.p12 chr16: 89,748,641-89,816,625 FANCA
    nsv4716505copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,816,311-89,883,065 , GRCh38.p12 chr16: 89,749,903-89,816,657 FANCA
    nsv6289814copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,818,265-89,883,065 , GRCh38.p12 chr16: 89,751,857-89,816,657 FANCA
    nsv4450242copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,818,536-89,883,033 , GRCh38 chr16: 89,752,128-89,816,625 FANCA
    nsv4716578copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,818,631-89,883,065 , GRCh38.p12 chr16: 89,752,223-89,816,657 FANCA
    nsv7137127copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,818,649-89,883,044 , GRCh38.p12 chr16: 89,752,241-89,816,636 FANCA
    nsv4682715copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr14: 45,605,235-45,669,211 , GRCh38.p12 chr14: 45,136,032-45,200,008 FANCM
    nsv6289948copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,820,416-89,883,065 , GRCh38.p12 chr16: 89,754,008-89,816,657 FANCA
    nsv6309898copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,818,536-89,877,489 , GRCh38.p12 chr16: 89,752,128-89,811,081 FANCA
    nsv4346184copy number variation1nstd102humanPathogenic GRCh38 chr16: 89,749,731-89,808,368 , GRCh37 chr16: 89,816,138-89,874,775 FANCA
    nsv4716420copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,816,311-89,874,701 , GRCh38.p12 chr16: 89,749,903-89,808,293 FANCA
    nsv6309900copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,824,975-89,883,033 , GRCh38.p12 chr16: 89,758,567-89,816,625 FANCA
    nsv6309897copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,818,526-89,874,795 , GRCh38.p12 chr16: 89,752,118-89,808,387 FANCA
    nsv4681916copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,818,536-89,874,785 , GRCh38.p12 chr16: 89,752,128-89,808,377 FANCA
    nsv4716520copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,825,114-89,880,927 , GRCh38.p12 chr16: 89,758,706-89,814,519 FANCA
    nsv4681407copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,828,347-89,883,024 , GRCh38.p12 chr16: 89,761,939-89,816,616 FANCA
    nsv4346335copy number variation1nstd102humanPathogenic GRCh38 chr16: 89,758,580-89,811,074 , GRCh37 chr16: 89,824,985-89,877,479 FANCA
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