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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904295copy number variation1nstd209human GRCh38 chr6: 151,297,015-151,302,638 , GRCh37.p13 chr6: 151,618,150-151,623,773 AKAP12, RNY4P20
    nsv5844661copy number variation1nstd209human GRCh38 chr6: 151,297,109-151,302,677 , GRCh37.p13 chr6: 151,618,244-151,623,812 AKAP12, RNY4P20
    nsv5682832mobile element insertion1nstd211human GRCh38 chr6: 151,297,036-151,297,036 , GRCh37.p13 chr6: 151,618,171-151,618,171 AKAP12, RNY4P20
    nsv5468288copy number variation1nstd206human GRCh38 chr6: 151,295,471-151,298,123 , GRCh37.p13 chr6: 151,616,606-151,619,258 RNY4P20, AKAP12
    nsv5467446copy number variation1nstd206human GRCh38 chr6: 151,296,995-151,302,661 , GRCh37.p13 chr6: 151,618,130-151,623,796 RNY4P20, AKAP12
    nsv5455805copy number variation1nstd206human GRCh38 chr6: 151,296,683-151,297,446 , GRCh37.p13 chr6: 151,617,818-151,618,581 AKAP12, RNY4P20
    nsv5329852translocation1nstd200human GRCh37 chr6: 151,618,152-151,618,152 , GRCh37 chr6: 151,623,774-151,623,774 , GRCh38.p12 chr6: 151,297,017-151,297,017 , GRCh38.p12 chr6: 151,302,639-151,302,639 AKAP12, RNY4P20
    nsv5315587copy number variation1nstd204human GRCh37.p13 chr6: 151,618,150-151,623,775 , GRCh38.p13 chr6: 151,297,015-151,302,640 AKAP12, RNY4P20
    nsv5236987copy number variation1nstd204human GRCh38.p13 chr6: 151,296,992-151,302,427 , GRCh37.p13 chr6: 151,618,127-151,623,562 AKAP12, RNY4P20
    nsv4943416copy number variation1nstd200human GRCh38 chr6: 151,297,017-151,302,639 , GRCh37.p13 chr6: 151,618,152-151,623,774 RNY4P20, AKAP12
    nsv4810933copy number variation1nstd200human GRCh37 chr6: 151,611,003-151,618,776 , GRCh38.p12 chr6: 151,289,868-151,297,641 RNY4P20, AKAP12
    nsv4729446copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 151,472,860-154,839,846 , GRCh38.p12 chr6: 151,151,725-154,518,712 ESR1, OPRM1, 45 more genes
    nsv4729213copy number variation1nstd102humanUncertain significance GRCh37 chr6: 151,121,109-151,664,579 , GRCh38.p12 chr6: 150,799,973-151,343,444 RNU6-302P, RPL32P16, 12 more genes
    nsv4679583copy number variation1nstd189human GRCh37.p13 chr6: 151,158,719-151,911,705 , GRCh38.p12 chr6: 150,837,583-151,590,570 AKAP12, MTHFD1L, 16 more genes
    nsv4675234copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929 RNU7-3P, HSPD1P16, 86 more genes
    nsv4456488copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222 PDCL3P5, SYTL3, 176 more genes
    nsv4455110copy number variation1nstd102humanUncertain significance GRCh37 chr6: 151,125,814-151,676,908 , GRCh38.p12 chr6: 150,804,678-151,355,773 ARL4AP5, MTHFD1L, 12 more genes
    nsv4436131complex substitution1nstd102humanPathogenic GRCh38.p12 chr6: 151,122,197-170,745,979 , GRCh37 chr6: 151,443,333-171,115,067 ACAT2, CCR6, 303 more genes
    nsv4403833copy number variation1nstd174human GRCh37 chr6: 151,618,001-151,624,000 , GRCh38.p12 chr6: 151,296,866-151,302,865 RNY4P20, AKAP12
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
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