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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075103inversion1nstd229human GRCh38 chr20: 48,844,229-55,780,453 , GRCh37.p13 chr20: 47,460,766-54,355,509 RPL12P4, LOC105372664, 113 more genes
    nsv7065344inversion1nstd229human GRCh38 chr20: 49,128,244-52,291,086 , GRCh37.p13 chr20: 47,744,781-50,907,625 PARD6B, LOC105372657, 77 more genes
    nsv7064075inversion1nstd229human GRCh38 chr20: 49,009,324-55,851,498 , GRCh37.p13 chr20: 47,625,861-54,426,554 DPM1, KCNG1, 115 more genes
    nsv7028111copy number variation1nstd229human GRCh38 chr20: 49,878,701-50,092,300 , GRCh37.p13 chr20: 48,495,238-48,708,837 SPATA2, UBE2V1, 10 more genes
    nsv7022636copy number variation1nstd229human GRCh38 chr20: 50,042,003-50,056,377 , GRCh37.p13 chr20: 48,658,540-48,672,914 TRERNA1, LOC105372655
    nsv7020409copy number variation1nstd229human GRCh38 chr20: 49,428,501-51,120,300 , GRCh37.p13 chr20: 48,045,038-49,736,837 LOC100421569, RNU6-147P, 54 more genes
    nsv6638039copy number variation1nstd102humanUncertain significance GRCh37 chr20: 48,352,572-48,766,664 , GRCh38.p12 chr20: 49,736,035-50,150,127 KRT18P4, LOC105372655, 16 more genes
    nsv6134303copy number variation1nstd213human GRCh37 chr20: 48,330,000-49,920,001 , GRCh38.p12 chr20: 49,713,463-51,303,464 KCNG1, PTPN1, 51 more genes
    nsv6133823copy number variation1nstd213human GRCh37 chr20: 47,890,000-48,840,001 , GRCh38.p12 chr20: 49,273,463-50,223,464 PTGIS, ZNFX1, 33 more genes
    nsv4285254copy number variation1nstd166human GRCh37.p13 chr20: 48,658,540-48,672,914 , GRCh38.p12 chr20: 50,042,003-50,056,377 TRERNA1, LOC105372655
    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
    nsv3918469copy number variation1nstd102humanLikely pathogenic NCBI36 chr20: 48,039,067-49,545,590 , GRCh37 chr20: 48,605,660-50,112,183 , GRCh38 chr20: 49,989,123-51,495,645 CEBPB, KCNG1, 40 more genes
    nsv3916972copy number variation1nstd102humanPathogenic GRCh38 chr20: 49,947,237-55,875,406 , NCBI36 chr20: 47,997,181-53,883,869 , GRCh37 chr20: 48,563,774-54,450,462 UBE2V1, KRT18P4, 87 more genes
    nsv3915867copy number variation1nstd102humanPathogenic GRCh37 chr20: 48,347,613-49,819,103 , GRCh38 chr20: 49,731,076-51,202,566 , NCBI36 chr20: 47,781,020-49,252,510 PEDS1-UBE2V1, SLC9A8, 48 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
    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
    nsv3908507copy number variation1nstd102humanPathogenic GRCh37 chr20: 47,627,844-52,045,480 , GRCh38.p12 chr20: 49,011,307-53,428,941 LOC100419570, KCNB1, 93 more genes
    nsv3907741copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 47,726,521-50,427,649 , GRCh38.p12 chr20: 49,109,984-51,811,110 CEBPB, KCNB1, 70 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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