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Items: 1 to 20 of 284

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903410copy number variation1nstd209human GRCh38 chr6: 4,056,147-4,056,235 , GRCh37.p13 chr6: 4,056,381-4,056,469 FAM217A, PRPF4B
    nsv5890742copy number variation1nstd209human GRCh38 chr6: 4,050,007-4,050,325 , GRCh37.p13 chr6: 4,050,241-4,050,559 PRPF4B, FAM217A
    nsv5714728mobile element insertion1nstd211human GRCh38 chr6: 4,050,326-4,050,326 , GRCh37.p13 chr6: 4,050,560-4,050,560 FAM217A, PRPF4B
    nsv5683491mobile element insertion2nstd211human GRCh38 chr6: 4,074,950-4,074,950 , GRCh37.p13 chr6: 4,075,184-4,075,184 FAM217A
    nsv5567681copy number variation1nstd207human GRCh38 chr6: 4,050,007-4,050,325 , GRCh37.p13 chr6: 4,050,241-4,050,559 PRPF4B, FAM217A
    nsv5469382copy number variation1nstd206human GRCh38 chr6: 4,056,147-4,056,245 , GRCh37.p13 chr6: 4,056,381-4,056,479 FAM217A, PRPF4B
    nsv5467091copy number variation1nstd206human GRCh38 chr6: 4,050,023-4,050,326 , GRCh37.p13 chr6: 4,050,257-4,050,560 FAM217A, PRPF4B
    nsv5460866copy number variation1nstd206human GRCh38 chr6: 4,086,302-4,090,342 , GRCh37.p13 chr6: 4,086,536-4,090,576 FAM217A, TEX56P
    nsv5399583mobile element insertion1nstd206human GRCh38 chr6: 4,074,950-4,075,001 , GRCh37.p13 chr6: 4,075,184-4,075,235 FAM217A
    nsv5384928mobile element deletion2nstd186human GRCh37 chr6: 4,050,257-4,050,560 , GRCh38.p12 chr6: 4,050,023-4,050,326 FAM217A, PRPF4B
    nsv5369168translocation1nstd200human GRCh38 chr6: 4,060,178-4,060,178 , GRCh38 chr6: 4,060,108-4,060,108 , GRCh37.p13 chr6: 4,060,342-4,060,342 , GRCh37.p13 chr6: 4,060,412-4,060,412 FAM217A, PRPF4B
    nsv5201092mobile element deletion1nstd204human GRCh37.p13 chr6: 4,050,257-4,050,560 , GRCh38.p13 chr6: 4,050,023-4,050,326 FAM217A, PRPF4B
    nsv5186333mobile element insertion1nstd203human GRCh38 chr6: 4,073,615-4,073,627 , GRCh37.p13 chr6: 4,073,849-4,073,861 FAM217A
    nsv5180658mobile element insertion1nstd203human GRCh38 chr6: 4,084,107-4,084,117 , GRCh37.p13 chr6: 4,084,341-4,084,351 FAM217A, TEX56P
    nsv5086465mobile element insertion1nstd203human GRCh38 chr6: 4,074,513-4,074,527 , GRCh37.p13 chr6: 4,074,747-4,074,761 FAM217A
    nsv5080644mobile element insertion1nstd203human GRCh38 chr6: 4,074,936-4,074,950 , GRCh37.p13 chr6: 4,075,170-4,075,184 FAM217A
    nsv4949376copy number variation1nstd200human GRCh38 chr6: 4,061,448-4,242,124 , GRCh37.p13 chr6: 4,061,682-4,242,358 ECI2, TEX56P, 6 more genes
    nsv4883406mobile element deletion1nstd200human GRCh38 chr6: 4,050,023-4,050,326 , GRCh37.p13 chr6: 4,050,257-4,050,560 PRPF4B, FAM217A
    nsv4778500mobile element deletion1nstd200human GRCh37 chr6: 4,076,279-4,076,583 , GRCh38.p12 chr6: 4,076,045-4,076,349 FAM217A
    nsv4778499mobile element deletion1nstd200human GRCh37 chr6: 4,050,257-4,050,560 , GRCh38.p12 chr6: 4,050,023-4,050,326 FAM217A, PRPF4B
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