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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5677578mobile element insertion2nstd211human GRCh38 chr2: 185,736,960-185,736,960 , GRCh37.p13 chr2: 186,601,687-186,601,687 FSIP2, FSIP2-AS2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5439030copy number variation1nstd206human GRCh38 chr2: 185,681,591-185,837,309 , GRCh37.p13 chr2: 186,546,318-186,702,036 , LOC100420895, 3 more genes
    nsv5438338copy number variation1nstd206human GRCh38 chr2: 185,735,489-185,735,806 , GRCh37.p13 chr2: 186,600,216-186,600,533 FSIP2-AS2
    nsv5412419mobile element insertion1nstd206human GRCh38 chr2: 185,736,960-185,737,011 , GRCh37.p13 chr2: 186,601,687-186,601,738 FSIP2-AS2, FSIP2
    nsv5287852copy number variation1nstd204human GRCh38.p13 chr2: 182,396,620-186,452,557 , GRCh37.p13 chr2: 183,261,347-187,317,284 , LINC01473, 36 more genes
    nsv5203383copy number variation1nstd204human GRCh38.p13 chr2: 183,941,201-186,452,500 , GRCh37.p13 chr2: 184,805,928-187,317,227 , RPL21P32, 23 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4928975copy number variation1nstd200human GRCh38 chr2: 185,736,698-185,743,731 , GRCh37.p13 chr2: 186,601,425-186,608,458 FSIP2-AS2, FSIP2
    nsv4928974copy number variation1nstd200human GRCh38 chr2: 185,714,574-185,732,777 , GRCh37.p13 chr2: 186,579,301-186,597,504 , FSIP2-AS2
    nsv4928960copy number variation1nstd200human GRCh38 chr2: 183,274,674-186,048,525 , GRCh37.p13 chr2: 184,139,402-186,913,252 , LOC107985832, 21 more genes
    nsv4916244copy number variation1nstd200human GRCh38 chr2: 185,728,211-185,728,311 , GRCh37.p13 chr2: 186,592,938-186,593,038 , FSIP2-AS2
    nsv4916242copy number variation1nstd200human GRCh38 chr2: 185,662,649-185,729,639 , GRCh37.p13 chr2: 186,527,376-186,594,366 , FSIP2-AS2
    nsv4916238copy number variation1nstd200human GRCh38 chr2: 185,574,661-186,006,700 , GRCh37.p13 chr2: 186,439,388-186,871,427 , FSIP2, 5 more genes
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4804454copy number variation1nstd200human GRCh37 chr2: 183,261,357-187,317,275 , GRCh38.p12 chr2: 182,396,630-186,452,548 , LOC107985832, 36 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728143copy number variation1nstd102humanLikely benign GRCh37 chr2: 186,505,306-186,682,290 , GRCh38.p12 chr2: 185,640,579-185,817,563 FSIP2-AS2, FSIP2-AS1, 1 more genes
    nsv4685593copy number variation1nstd102humannot provided GRCh37 chr2: 183,764,930-187,399,282 , GRCh38.p12 chr2: 182,900,202-186,534,555 ZC3H15, ZNF804A, 29 more genes
    nsv4674757copy number variation1nstd102humanPathogenic GRCh37 chr2: 174,690,039-195,521,582 , GRCh38.p12 chr2: 173,825,311-194,656,858 OSBPL6, DNAJC19P5, 256 more genes
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