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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144682insertion1nstd232human GRCh37.p13 chr10: 43,288,593-43,288,593 , GRCh38.p12 chr10: 42,793,145-42,793,145 BMS1
    nsv7143767copy number variation1nstd232human GRCh37.p13 chr10: 43,315,869-43,315,951 , GRCh38.p12 chr10: 42,820,421-42,820,503 BMS1
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7071643inversion1nstd229human GRCh38 chr10: 42,146,783-43,722,055 , GRCh37.p13 chr10: 42,642,231-44,217,503 RNU6ATAC11P, EIF3LP2, 48 more genes
    nsv6892825copy number variation1nstd229human GRCh38 chr10: 42,805,831-42,809,845 , GRCh37.p13 chr10: 43,301,279-43,305,293 BMS1
    nsv6883580copy number variation1nstd229human GRCh38 chr10: 42,792,424-46,796,570 , GRCh37.p13 chr10: 43,287,872-46,224,333 RASSF4, AGAP14P, 107 more genes
    nsv6883509copy number variation1nstd229human GRCh38 chr10: 42,788,951-42,806,912 , GRCh37.p13 chr10: 43,284,399-43,302,360 BMS1
    nsv6635492copy number variation1nstd227human GRCh38.p12 chr10: 42,186,685-42,879,460 , GRCh37 chr10: 42,682,133-43,374,908 ZNF33B, BMS1, 22 more genes
    nsv6635361copy number variation1nstd227human GRCh38.p12 chr10: 42,230,215-42,879,460 , GRCh37 chr10: 42,725,663-43,374,908 ZNF33B, BMS1, 22 more genes
    nsv6452941copy number variation1nstd223human GRCh38 chr10: 42,792,279-42,793,308 , GRCh37.p13 chr10: 43,287,727-43,288,756 BMS1
    nsv6446056copy number variation1nstd223human GRCh38 chr10: 42,740,574-42,887,602 , GRCh37.p13 chr10: 43,236,022-43,383,050 LOC283028, LINC02623, 4 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6276424insertion1nstd214human GRCh38 chr10: 42,781,771-42,781,771 , GRCh37.p13 chr10: 43,277,219-43,277,219 BMS1
    nsv6089538insertion1nstd212human GRCh38 chr10: 42,809,010-42,809,010 , GRCh37.p13 chr10: 43,304,458-43,304,458 BMS1
    nsv5723004mobile element insertion1nstd211human GRCh38 chr10: 42,816,829-42,816,829 , GRCh37.p13 chr10: 43,312,277-43,312,277 BMS1
    nsv5644335insertion1nstd207human GRCh38 chr10: 42,834,618-42,834,618 , GRCh37.p13 chr10: 43,330,066-43,330,066 BMS1
    nsv5630985insertion1nstd207human GRCh38 chr10: 42,830,350-42,830,350 , GRCh37.p13 chr10: 43,325,798-43,325,798 BMS1
    nsv5490268copy number variation1nstd206human GRCh38 chr10: 42,827,403-42,828,417 , GRCh37.p13 chr10: 43,322,851-43,323,865 BMS1
    nsv5489882copy number variation1nstd206human GRCh38 chr10: 42,783,594-42,783,736 , GRCh37.p13 chr10: 43,279,042-43,279,184 BMS1
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