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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv5972231insertion1nstd209human GRCh38 chr12: 6,794,785-6,794,785 , GRCh37.p13 chr12: 6,903,951-6,903,951 CD4
    nsv5969912insertion1nstd209human GRCh38 chr12: 6,788,361-6,788,361 , GRCh37.p13 chr12: 6,897,527-6,897,527 CD4
    nsv5927069copy number variation1nstd209human GRCh38 chr12: 6,798,217-6,798,472 , GRCh37.p13 chr12: 6,907,383-6,907,580 CD4
    nsv5660561insertion1nstd207human GRCh38 chr12: 6,820,694-6,820,694 , GRCh37.p13 chr12|NW_003871083.2: 22,280-22,280 , GRCh37.p13 chr12: 6,929,860-6,929,860 GPR162, CD4
    nsv5603310copy number variation1nstd207human GRCh38 chr12: 6,798,217-6,798,472 , GRCh37.p13 chr12: 6,907,383-6,907,580 CD4
    nsv5564211copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,438,478-7,362,819 , GRCh38.p12 chr12: 6,329,312-7,210,223 GPR162, SCARNA11, 68 more genes
    nsv5505056copy number variation1nstd206human GRCh38 chr12: 6,802,549-6,812,033 , GRCh37.p13 chr12|NW_003871083.2: 4,135-13,619 , GRCh37.p13 chr12: 6,911,715-6,921,199 CD4
    nsv5503112copy number variation1nstd206human GRCh38 chr12: 6,798,218-6,798,473 , GRCh37.p13 chr12: 6,907,384-6,907,580 CD4
    nsv5391304copy number variation1nstd186human GRCh37 chr12: 6,907,384-6,907,580 , GRCh38.p12 chr12: 6,798,218-6,798,414 CD4
    nsv5390618copy number variation1nstd186human GRCh37 chr12: 6,907,384-6,907,639 , GRCh38.p12 chr12: 6,798,218-6,798,473 CD4
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5319908copy number variation1nstd204human GRCh38.p13 chr12: 6,798,037-6,798,507 , GRCh37.p13 chr12: 6,907,203-6,907,614 CD4
    nsv5313620copy number variation1nstd204human GRCh38.p13 chr12: 6,803,116-6,807,353 , GRCh37.p13 chr12: 6,912,282-6,916,519 , GRCh37.p13 chr12|NW_003871083.2: 4,702-8,939 CD4
    nsv5279702copy number variation1nstd204human GRCh38.p13 chr12: 6,507,601-6,909,400 , GRCh37.p13 chr12: 6,616,767-6,907,580 ING4, LPAR5, 30 more genes
    nsv5278422copy number variation1nstd204human GRCh38.p13 chr12: 6,804,925-6,807,394 , GRCh37.p13 chr12: 6,914,091-6,916,560 , GRCh37.p13 chr12|NW_003871083.2: 6,511-8,980 CD4
    nsv5275370copy number variation1nstd204human GRCh38.p13 chr12: 6,798,201-6,798,500 , GRCh37.p13 chr12: 6,907,367-6,907,580 CD4
    nsv5264559copy number variation1nstd204human GRCh38.p13 chr12: 6,803,505-6,806,857 , GRCh37.p13 chr12|NW_003871083.2: 5,091-8,443 , GRCh37.p13 chr12: 6,912,671-6,916,023 CD4
    nsv5261405copy number variation1nstd204human GRCh38.p13 chr12: 6,720,401-6,891,700 , GRCh37.p13 chr12|NW_003871083.2: 1-93,284 , GRCh37.p13 chr12: 6,907,581-7,000,864 DSTNP2, RPL13P5, 14 more genes
    nsv5139035mobile element insertion1nstd203human GRCh38 chr12: 6,811,837-6,811,837 , GRCh37.p13 chr12: 6,921,003-6,921,003 , GRCh37.p13 chr12|NW_003871083.2: 13,423-13,423 CD4
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