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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7069270inversion1nstd229human GRCh38 chr20: 47,330,519-47,384,590 , GRCh37.p13 chr20: 45,959,263-46,013,334 ZMYND8, LOC101927377, 1 more genes
    nsv7035022copy number variation1nstd229human GRCh38 chr20: 46,694,955-48,915,753 , GRCh37.p13 chr20: 45,323,594-47,532,290 GAPDHP54, RNU6-563P, 38 more genes
    nsv7033583copy number variation1nstd229human GRCh38 chr20: 47,345,225-47,582,240 , GRCh37.p13 chr20: 45,973,969-46,210,984 RPL35AP, RNU6-563P, 5 more genes
    nsv6291460copy number variation1nstd102humanUncertain significance GRCh37 chr20: 45,626,379-46,257,019 , GRCh38.p12 chr20: 46,997,740-47,628,275 MIR3616, LOC100131496, 10 more genes
    nsv6290315copy number variation1nstd102humanPathogenic GRCh37 chr20: 42,985,044-48,599,046 , GRCh38.p12 chr20: 44,356,404-49,982,509 PABPC1L, LOC107985401, 170 more genes
    nsv6134301copy number variation1nstd213human GRCh37 chr20: 45,870,000-46,040,001 , GRCh38.p12 chr20: 47,241,256-47,411,257 ZMYND8, LOC100131496, 2 more genes
    nsv6133817copy number variation1nstd213human GRCh37 chr20: 45,780,000-46,470,001 , GRCh38.p12 chr20: 47,151,361-47,841,257 EYA2, ZMYND8, 14 more genes
    nsv5292479copy number variation1nstd204human GRCh37.p13 chr20: 45,897,945-46,153,944 , GRCh38.p13 chr20: 47,269,201-47,525,200 NCOA3, ZMYND8, 6 more genes
    nsv4853714copy number variation1nstd200human GRCh37 chr20: 45,982,849-45,983,735 , GRCh38.p12 chr20: 47,354,105-47,354,991 ZMYND8, LOC101927377
    nsv4674805copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 34,980,430-46,806,549 , GRCh38.p12 chr20: 36,352,027-48,177,806 ADA, BPI, 266 more genes
    nsv4620885copy number variation1nstd183human GRCh37 chr20: 45,980,206-45,986,421 , GRCh38.p12 chr20: 47,351,462-47,357,677 LOC101927377, ZMYND8
    nsv4620665copy number variation1nstd183human GRCh37 chr20: 45,978,466-46,365,571 , GRCh38.p12 chr20: 47,349,722-47,736,827 NCOA3, ZMYND8, 7 more genes
    nsv4536379copy number variation1nstd166human GRCh37.p13 chr20: 45,980,999-46,225,000 , GRCh38.p12 chr20: 47,352,255-47,596,256 NCOA3, ZMYND8, 5 more genes
    nsv3920218copy number variation1nstd102humanPathogenic GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118 MIR3646, NPEPL1, 1310 more genes
    nsv3915005copy number variation1nstd102humanPathogenic NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321 FTLP1, RNA5SP487, 472 more genes
    nsv3912723copy number variation1nstd102humanPathogenic NCBI36 chr20: 30,288,202-45,731,170 , GRCh37.p13 chr20: 30,824,541-46,297,763 , GRCh38.p12 chr20: 32,236,738-47,669,019 LOC107985448, LOC105372613, 370 more genes
    nsv3910818copy number variation1nstd102humanUncertain significance NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167 RNA5SP481, LOC105372625, 855 more genes
    nsv3910049copy number variation1nstd102humanPathogenic NCBI36 chr20: 33,289,165-45,693,969 , GRCh37 chr20: 33,825,749-46,260,562 , GRCh38 chr20: 35,237,946-47,631,818 NDUFB4P10, EIF4EBP2P1, 291 more genes
    nsv3905072copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435 LRRN4, SNRPB, 1313 more genes
    nsv3896520copy number variation1nstd102humanPathogenic GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110 COMMD7, RNU7-6P, 1311 more genes
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