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Items: 1 to 20 of 125

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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
    nsv6733657copy number variation1nstd229human GRCh38 chr3: 194,445,499-194,561,633 , GRCh37.p13 chr3: 194,166,228-194,282,362 RNU6-1101P, RPL23AP93, 2 more genes
    nsv6732659copy number variation1nstd229human GRCh38 chr3: 194,391,019-194,558,345 , GRCh37.p13 chr3: 194,111,748-194,279,074 ATP13A3, ATP13A3-DT, 2 more genes
    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
    nsv6731368copy number variation1nstd229human GRCh38 chr3: 194,478,867-194,487,498 , GRCh37.p13 chr3: 194,199,596-194,208,227 ATP13A3-DT, ATP13A3
    nsv6721364copy number variation1nstd229human GRCh38 chr3: 194,439,395-194,502,189 , GRCh37.p13 chr3: 194,160,124-194,222,918 ATP13A3-DT, ATP13A3
    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
    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
    nsv6135007copy number variation1nstd213human GRCh37 chr3: 194,040,000-194,250,001 , GRCh38.p12 chr3: 194,322,211-194,529,272 CPN2, GP5, 3 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
    nsv4925023copy number variation1nstd200human GRCh38 chr3: 194,463,701-194,533,410 , GRCh37.p13 chr3: 194,184,430-194,254,139 ATP13A3, ATP13A3-DT, 1 more genes
    nsv4805098copy number variation1nstd200human GRCh37 chr3: 194,184,430-194,254,139 , GRCh38.p12 chr3: 194,463,701-194,533,410 ATP13A3, ATP13A3-DT, 1 more genes
    nsv4685587copy number variation1nstd102humannot provided GRCh37 chr3: 194,161,542-194,998,084 , GRCh38.p12 chr3: 194,440,813-195,277,355 RPL23AP93, LSG1, 22 more genes
    nsv4596324copy number variation1nstd183human GRCh37 chr3: 193,962,049-194,571,078 , GRCh38.p12 chr3: 194,244,260-194,850,349 , LINC01968, 20 more genes
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