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Items: 1 to 20 of 478

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147024insertion1nstd232human GRCh37.p13 chr9: 139,108,570-139,108,570 , GRCh38.p12 chr9: 136,216,724-136,216,724 QSOX2
    nsv7098071copy number variation2nstd102humanPathogenic GRCh37 chr9: 139,089,171-141,016,451 , GRCh38.p12 chr9: 136,197,325-138,121,999 NPDC1, LOC101928786, 108 more genes
    nsv7098070copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,392,557-141,016,451 , GRCh38.p12 chr9: 135,500,711-138,121,999 STPG3-AS1, CACNA1B-AS1, 132 more genes
    nsv7098066copy number variation4nstd102humanUncertain significance GRCh37 chr9: 135,139,626-140,034,216 , GRCh38.p12 chr9: 132,264,239-137,139,764 LINC02692, SNORD141A, 181 more genes
    nsv7097937copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,089,161-139,096,868 , GRCh38.p12 chr9: 136,197,315-136,205,022 QSOX2, LHX3
    nsv7097697copy number variation1nstd102humanUncertain significance GRCh37 chr9: 136,218,768-141,016,451 , GRCh38.p12 chr9: 133,351,913-138,121,999 LOC105376326, LOC107987143, 186 more genes
    nsv7097690copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,087,402-141,016,451 , GRCh38.p12 chr9: 128,325,123-138,121,999 REXO4, TOR1B, 324 more genes
    nsv7093414copy number variation1nstd102humanPathogenic GRCh38 chr9: 134,932,722-137,269,957 , GRCh37.p13 chr9: 137,824,568-140,164,409 LHX3, FUT7, 121 more genes
    nsv7075268inversion1nstd229human GRCh38 chr9: 128,672,751-137,526,572 , GRCh37.p13 chr9: 131,435,030-140,421,024 PNPLA7, NSMF, 293 more genes
    nsv7075196inversion1nstd229human GRCh38 chr9: 130,990,409-137,053,229 , GRCh37.p13 chr9: 133,865,796-139,947,681 LINC02907, LCN1, 196 more genes
    nsv7070027inversion1nstd229human GRCh38 chr9: 135,876,745-136,834,735 , GRCh37.p13 chr9: 138,768,591-139,729,187 LOC107987142, LCN8, 48 more genes
    nsv7059760inversion1nstd229human GRCh38 chr9: 130,985,407-137,050,712 , GRCh37.p13 chr9: 133,860,794-139,945,164 LCN10, RAPGEF1, 196 more genes
    nsv6896598copy number variation1nstd229human GRCh38 chr9: 136,208,175-136,228,892 , GRCh37.p13 chr9: 139,100,021-139,120,738 QSOX2
    nsv6889325copy number variation1nstd229human GRCh38 chr9: 136,229,246-136,236,522 , GRCh37.p13 chr9: 139,121,092-139,128,368 QSOX2
    nsv6887498copy number variation1nstd229human GRCh38 chr9: 136,214,667-136,443,437 , GRCh37.p13 chr9: 139,106,513-139,337,889 DKFZP434A062, QSOX2, 9 more genes
    nsv6885800copy number variation1nstd229human GRCh38 chr9: 136,239,360-136,243,314 , GRCh37.p13 chr9: 139,131,206-139,135,160 QSOX2
    nsv6884507copy number variation1nstd229human GRCh38 chr9: 135,999,993-136,390,538 , GRCh37.p13 chr9: 138,891,839-139,284,990 LINC02846, CCDC187, 10 more genes
    nsv6881641copy number variation1nstd229human GRCh38 chr9: 136,213,475-136,213,561 , GRCh37.p13 chr9: 139,105,321-139,105,407 QSOX2
    nsv6881132copy number variation1nstd229human GRCh38 chr9: 136,236,906-136,261,424 , GRCh37.p13 chr9: 139,136,890-139,153,270 , GRCh37.p13 chr9|NW_003315926.1: 1-16,381 CCDC187, QSOX2
    nsv6637952copy number variation1nstd102humanUncertain significance GRCh37 chr9: 138,929,784-139,252,520 , GRCh38.p12 chr9: 136,037,938-136,358,068 LINC02846, GPSM1, 8 more genes
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