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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924814copy number variation1nstd209human GRCh38 chr6: 166,162,673-166,162,798 , GRCh37.p13 chr6: 166,576,161-166,576,286 TBXT
    nsv5579808copy number variation1nstd207human GRCh38 chr6: 166,162,673-166,162,798 , GRCh37.p13 chr6: 166,576,161-166,576,286 TBXT
    nsv4968655copy number variation1nstd200human GRCh38 chr6: 165,587,706-166,398,601 , GRCh37.p13 chr6: 166,001,194-166,812,089 LOC105378115, TBXT, 19 more genes
    nsv4824887copy number variation1nstd200human GRCh37 chr6: 166,001,194-166,812,089 , GRCh38.p12 chr6: 165,587,706-166,398,601 GNG5P1, LOC107986668, 19 more genes
    nsv4730828copy number variation1nstd199human GRCh37 chr6: 166,576,168-166,576,295 , GRCh38.p12 chr6: 166,162,680-166,162,807 TBXT
    nsv4729645copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 166,083,476-170,919,482 , GRCh38.p12 chr6: 165,669,988-170,610,394 CCR6, GNG5P1, 118 more genes
    nsv4675923copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,452,035-170,919,482 , GRCh38.p12 chr6: 162,031,003-170,610,394 TRE-TTC15-1, LOC105378137, 148 more genes
    nsv4675281copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,661,108-170,919,482 , GRCh38.p12 chr6: 162,240,076-170,610,394 LOC105378127, LOC105378130, 148 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
    nsv4376081copy number variation1nstd173human GRCh37 chr6: 163,617,482-170,919,482 , GRCh38.p12 chr6: 163,196,450-170,610,394 , LOC107986550, 151 more genes
    nsv4349604copy number variation1nstd102humanPathogenic GRCh37 chr6: 166,517,762-170,919,470 , GRCh38.p12 chr6: 166,104,274-170,610,382 LOC105378145, FRMD1, 109 more genes
    nsv4347933copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 162,966,301-170,914,973 , GRCh38.p12 chr6: 162,545,269-170,605,885 CCR6, GNG5P1, 146 more genes
    nsv3924367copy number variation1nstd102humanUncertain significance GRCh37 chr6: 166,044,862-166,819,268 , GRCh38 chr6: 165,631,374-166,405,780 , NCBI36 chr6: 165,964,852-166,739,258 RNU6-153P, LOC100289495, 19 more genes
    nsv3923494copy number variation1nstd102humanUncertain significance GRCh37 chr6: 166,044,862-166,774,510 , GRCh38 chr6: 165,631,374-166,361,022 , NCBI36 chr6: 165,964,852-166,694,500 LOC105378115, GAPDHP72, 18 more genes
    nsv3923088copy number variation1nstd102humanPathogenic GRCh37 chr6: 160,246,945-170,921,089 , NCBI36 chr6: 160,166,935-170,763,014 , GRCh38 chr6: 159,825,913-170,612,001 DKFZp451B082, LOC107986548, 169 more genes
    nsv3922436copy number variation1nstd102humanPathogenic NCBI36 chr6: 163,526,015-170,896,992 , GRCh37.p13 chr6: 163,606,025-171,055,067 , GRCh38.p12 chr6: 163,184,993-170,745,979 LINC02538, PACRG-AS3, 145 more genes
    nsv3922220copy number variation1nstd102humanPathogenic NCBI36 chr6: 163,130,937-170,753,165 , GRCh38 chr6: 162,789,915-170,602,152 , GRCh37 chr6: 163,210,947-170,911,240 LOC105378114, LOC105378157, 143 more genes
    nsv3921695copy number variation1nstd102humanPathogenic GRCh38 chr6: 154,539,655-170,714,507 , NCBI36 chr6: 154,902,481-170,865,520 , GRCh37 chr6: 154,860,789-171,023,595 LOC105378128, LOC105378102, 255 more genes
    nsv3921491copy number variation1nstd102humanPathogenic NCBI36 chr6: 159,795,661-170,763,014 , GRCh38 chr6: 159,454,639-170,612,001 , GRCh37 chr6: 159,875,671-170,921,089 LOC102724357, LOC101929142, 183 more genes
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 UST-AS2, LOC729681, 394 more genes
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