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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148072copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 193,343,827-194,599,635 , GRCh38.p12 chr3: 193,626,038-194,878,906 CPN2, GP5, 36 more genes
    nsv7040982inversion1nstd229human GRCh38 chr3: 193,802,086-196,241,826 , GRCh37.p13 chr3: 193,519,875-195,968,697 CPN2, RNU6ATAC24P, 73 more genes
    nsv6737551copy number variation1nstd229human GRCh38 chr3: 194,665,458-194,831,295 , GRCh37.p13 chr3: 194,386,187-194,552,024 FAM151AP1, LSG1, 4 more genes
    nsv6734544copy number variation1nstd229human GRCh38 chr3: 194,685,668-194,685,721 , GRCh37.p13 chr3: 194,406,397-194,406,450 FAM43A
    nsv6731714copy number variation1nstd229human GRCh38 chr3: 192,378,501-195,488,100 , GRCh37.p13 chr3: 192,096,290-195,214,903 LSG1, MB21D2, 61 more genes
    nsv6730656copy number variation1nstd229human GRCh38 chr3: 194,685,008-194,744,439 , GRCh37.p13 chr3: 194,405,737-194,465,168 LOC105374292, FAM43A, 1 more genes
    nsv6730637copy number variation1nstd229human GRCh38 chr3: 194,688,539-194,697,923 , GRCh37.p13 chr3: 194,409,268-194,418,652 FAM43A
    nsv6729936copy number variation1nstd229human GRCh38 chr3: 194,595,632-194,782,335 , GRCh37.p13 chr3: 194,316,361-194,503,064 LINC01968, FAM43A, 6 more genes
    nsv6725145copy number variation1nstd229human GRCh38 chr3: 194,686,101-194,688,000 , GRCh37.p13 chr3: 194,406,830-194,408,729 FAM43A
    nsv6723830copy number variation1nstd229human GRCh38 chr3: 194,665,636-194,990,341 , GRCh37.p13 chr3: 194,386,365-194,711,070 LOC105374292, LSG1, 6 more genes
    nsv6636634copy number variation1nstd102humanUncertain significance GRCh37 chr3: 193,396,762-195,009,038 , GRCh38.p12 chr3: 193,678,973-195,288,309 LINC02036, LINC02026, 45 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6628936copy number variation1nstd224human GRCh37 chr3: 194,362,826-194,769,114 , GRCh38.p12 chr3: 194,642,097-195,048,385 LSG1, FAM43A, 7 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6313527copy number variation1nstd102humanUncertain significance GRCh37 chr3: 192,607,378-194,745,252 , GRCh38.p12 chr3: 192,889,589-195,024,523 LINC02036, HES1, 48 more genes
    nsv6290259copy number variation1nstd102humanPathogenic GRCh37 chr3: 189,608,636-197,532,175 , GRCh38.p12 chr3: 189,890,847-197,805,304 LINC01972, LINC02026, 174 more genes
    nsv6290248copy number variation1nstd102humanPathogenic GRCh37 chr3: 191,866,466-197,842,171 , GRCh38.p12 chr3: 192,148,677-198,115,300 PIGZ, LOC107986173, 156 more genes
    nsv5559488sequence alteration1nstd206human GRCh37.p13 chr3: 194,362,410-194,675,824 , GRCh38 chr3: 194,641,681-194,955,095 , LSG1, 6 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5449508copy number variation1nstd206human GRCh38 chr3: 194,433,000-194,791,574 , GRCh37.p13 chr3: 194,153,729-194,512,303 RNU6-1101P, FAM151AP1, 11 more genes
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