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Items: 1 to 20 of 78

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381779copy number variation1nstd102humanPathogenic GRCh37 chr6: 155,308,263-158,394,005 , GRCh38.p12 chr6: 154,987,129-157,972,973 TFB1M, ARID1B, 30 more genes
    nsv5310078copy number variation1nstd204human GRCh38.p13 chr6: 157,839,496-158,613,672 , GRCh37.p13 chr6: 158,260,528-159,034,704 CACYBPP3, SYNJ2, 14 more genes
    nsv5227727copy number variation1nstd204human GRCh38.p13 chr6: 157,887,852-157,890,054 , GRCh37.p13 chr6: 158,308,884-158,311,086 SNX9, SNX9-AS1
    nsv5173299mobile element insertion1nstd203human GRCh38 chr6: 157,891,810-157,891,815 , GRCh37.p13 chr6: 158,312,842-158,312,847 SNX9, SNX9-AS1
    nsv4945880copy number variation1nstd200human GRCh38 chr6: 157,839,506-158,613,666 , GRCh37.p13 chr6: 158,260,538-159,034,698 CACYBPP3, SYNJ2-IT1, 14 more genes
    nsv4824831copy number variation1nstd200human GRCh37 chr6: 158,260,538-159,034,698 , GRCh38.p12 chr6: 157,839,506-158,613,666 SNX9, SYNJ2-IT1, 14 more genes
    nsv4766814inversion1nstd199human GRCh37 chr6: 153,752,140-161,206,728 , GRCh38.p12 chr6: 153,431,005-160,785,696 , ACAT2, 111 more genes
    nsv4456892copy number variation1nstd102humanUncertain significance GRCh37 chr6: 155,426,680-158,863,541 , GRCh38.p12 chr6: 155,105,546-158,442,509 GTF2H5, TIAM2, 37 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
    nsv4455446copy number variation1nstd102humanUncertain significance GRCh37 chr6: 157,262,571-160,992,289 , GRCh38.p12 chr6: 156,941,437-160,571,257 LOC105378076, LOC107986663, 67 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
    nsv4385174copy number variation1nstd173human GRCh37 chr6: 158,311,995-158,377,370 , GRCh38.p12 chr6: 157,890,963-157,956,338 SNX9, SNX9-AS1, 2 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 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
    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
    nsv3918864copy number variation1nstd102humanPathogenic GRCh38 chr6: 157,827,805-159,726,548 , NCBI36 chr6: 158,168,825-160,067,570 , GRCh37 chr6: 158,248,837-160,147,580 GTF2H5, SNORA116, 39 more genes
    nsv3916405copy number variation1nstd102humanPathogenic NCBI36 chr6: 150,744,068-159,894,974 , GRCh38 chr6: 150,381,239-159,553,952 , GRCh37 chr6: 150,702,375-159,974,984 LOC112267968, ARMT1, 126 more genes
    nsv3916251copy number variation1nstd102humanPathogenic GRCh38 chr6: 155,378,049-163,133,499 , NCBI36 chr6: 155,740,875-163,474,521 , GRCh37 chr6: 155,699,183-163,554,531 MAP3K4, LOC112267977, 99 more genes
    nsv3914565copy number variation1nstd102humanLikely pathogenic NCBI36 chr6: 154,541,790-159,361,389 , GRCh37 chr6: 154,500,098-159,441,401 , GRCh38 chr6: 154,178,964-159,020,369 OPRM1, DYNLT1, 67 more genes
    nsv3913213copy number variation1nstd102humanPathogenic GRCh38 chr6: 154,118,058-170,602,152 , NCBI36 chr6: 154,480,885-170,753,165 , GRCh37 chr6: 154,439,193-170,911,240 LDHAL6FP, QKI, 258 more genes
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