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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112778copy number variation1nstd102humanPathogenic GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273 LINC01742, MTCO2P1, 253 more genes
    nsv5881683copy number variation1nstd209human GRCh38 chr20: 56,525,687-56,536,614 , GRCh37.p13 chr20: 55,100,743-55,111,670 GCNT7, FAM209A, 1 more genes
    nsv5350492translocation1nstd200human GRCh38 chr20: 56,522,227-56,522,227 , GRCh38 chr20: 56,536,337-56,536,337 , GRCh37.p13 chr20: 55,097,283-55,097,283 , GRCh37.p13 chr20: 55,111,393-55,111,393 GCNT7, FAM209B
    nsv5293387copy number variation1nstd204human GRCh38.p13 chr20: 56,555,211-56,558,660 , GRCh37.p13 chr20: 55,130,267-55,133,716 FAM209B
    nsv5171675mobile element insertion1nstd203human GRCh38 chr20: 56,535,064-56,535,095 , GRCh37.p13 chr20: 55,110,120-55,110,151 FAM209B
    nsv5169810mobile element insertion1nstd203human GRCh38 chr20: 56,531,689-56,531,689 , GRCh37.p13 chr20: 55,106,745-55,106,745 FAM209A, FAM209B
    nsv5025751copy number variation1nstd200human GRCh38 chr20: 56,510,773-56,538,566 , GRCh37.p13 chr20: 55,085,829-55,113,622 RTF2, FAM209A, 2 more genes
    nsv5013302copy number variation1nstd200human GRCh38 chr20: 56,555,688-56,565,027 , GRCh37.p13 chr20: 55,130,744-55,140,083 FAM209B
    nsv5013301copy number variation1nstd200human GRCh38 chr20: 56,543,015-56,547,151 , GRCh37.p13 chr20: 55,118,071-55,122,207 FAM209B
    nsv5013300copy number variation1nstd200human GRCh38 chr20: 56,532,615-56,534,602 , GRCh37.p13 chr20: 55,107,671-55,109,658 FAM209A, FAM209B
    nsv5013299copy number variation1nstd200human GRCh38 chr20: 56,523,317-56,531,119 , GRCh37.p13 chr20: 55,098,373-55,106,175 FAM209B, GCNT7, 1 more genes
    nsv4865662copy number variation1nstd200human GRCh37 chr20: 55,104,014-55,109,099 , GRCh38.p12 chr20: 56,528,958-56,534,043 FAM209B, FAM209A
    nsv4853986copy number variation1nstd200human GRCh37 chr20: 55,118,071-55,122,207 , GRCh38.p12 chr20: 56,543,015-56,547,151 FAM209B
    nsv4853985copy number variation1nstd200human GRCh37 chr20: 55,098,373-55,106,175 , GRCh38.p12 chr20: 56,523,317-56,531,119 FAM209B, GCNT7, 1 more genes
    nsv4680243copy number variation1nstd189human GRCh37.p13 chr20: 55,056,882-55,294,109 , GRCh38.p12 chr20: 56,481,826-56,719,053 , TFAP2C, 9 more genes
    nsv4575062mobile element insertion1nstd166human GRCh37.p13 chr20: 55,130,544-55,130,544 , GRCh38.p12 chr20: 56,555,488-56,555,488 FAM209B
    nsv4513488mobile element insertion1nstd166human GRCh37.p13 chr20: 55,125,348-55,125,348 , GRCh38.p12 chr20: 56,550,292-56,550,292 FAM209B
    nsv4357849copy number variation1nstd102humanPathogenic GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528 RBM38, LAMA5, 192 more genes
    nsv4290322copy number variation1nstd166human GRCh37.p13 chr20: 55,130,744-55,140,083 , GRCh38.p12 chr20: 56,555,688-56,565,027 FAM209B
    nsv4290058copy number variation1nstd166human GRCh37.p13 chr20: 55,118,071-55,122,207 , GRCh38.p12 chr20: 56,543,015-56,547,151 FAM209B
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