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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5922663copy number variation1nstd209human GRCh38 chr6: 166,372,399-166,372,458 , GRCh37.p13 chr6: 166,785,887-166,785,946 MPC1
    nsv5363542translocation1nstd200human GRCh38 chr6: 166,383,725-166,383,725 , GRCh38 chr6: 166,379,691-166,379,691 , GRCh37.p13 chr6: 166,797,213-166,797,213 , GRCh37.p13 chr6: 166,793,179-166,793,179 MPC1
    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
    nsv4965931copy number variation1nstd200human GRCh38 chr6: 166,375,391-166,385,602 , GRCh37.p13 chr6: 166,788,879-166,799,090 MPC1
    nsv4965930copy number variation1nstd200human GRCh38 chr6: 166,368,506-166,369,336 , GRCh37.p13 chr6: 166,781,994-166,782,824 MPC1
    nsv4965929copy number variation1nstd200human GRCh38 chr6: 166,362,527-166,364,012 , GRCh37.p13 chr6: 166,776,015-166,777,500 MPC1
    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
    nsv4818039copy number variation1nstd200human GRCh37 chr6: 166,776,015-166,777,500 , GRCh38.p12 chr6: 166,362,527-166,364,012 MPC1
    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
    nsv4524506copy number variation1nstd166human GRCh37.p13 chr6: 166,781,995-166,782,823 , GRCh38.p12 chr6: 166,368,507-166,369,335 MPC1
    nsv4455397copy number variation1nstd102humanPathogenic GRCh37 chr6: 166,607,593-170,919,482 , GRCh38.p12 chr6: 166,194,105-170,610,394 TBP, LOC112267970, 108 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
    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
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