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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048284inversion1nstd229human GRCh38 chr6: 73,272,579-75,940,581 , GRCh37.p13 chr6: 73,982,302-76,650,298 RPL39P3, KHDC1, 45 more genes
    nsv7043838inversion1nstd229human GRCh38 chr6: 73,208,570-73,391,551 , GRCh37.p13 chr6: 73,918,293-74,101,274 RPSAP41, KHDC3L, 10 more genes
    nsv6792787copy number variation1nstd229human GRCh38 chr6: 73,321,495-73,329,277 , GRCh37.p13 chr6: 74,031,218-74,039,000 SDCBP2P1, PAICSP3
    nsv6790487copy number variation1nstd229human GRCh38 chr6: 73,006,301-73,863,300 , GRCh37.p13 chr6: 73,716,024-74,573,015 RBPMS2P1, SLC17A5, 24 more genes
    nsv6787789copy number variation1nstd229human GRCh38 chr6: 73,224,501-73,533,000 , GRCh37.p13 chr6: 73,934,224-74,242,723 DDX43, KHDC3L, 15 more genes
    nsv6784485copy number variation1nstd229human GRCh38 chr6: 73,256,414-73,487,243 , GRCh37.p13 chr6: 73,966,137-74,196,966 OOEP, RN7SL827P, 13 more genes
    nsv6780279copy number variation1nstd229human GRCh38 chr6: 73,319,073-73,326,394 , GRCh37.p13 chr6: 74,028,796-74,036,117 SDCBP2P1, PAICSP3
    nsv6634377copy number variation1nstd102humanPathogenic GRCh37 chr6: 71,105,038-75,200,617 , GRCh38.p12 chr6: 70,395,335-74,490,901 TXNP7, MTO1, 63 more genes
    nsv6573990inversion1nstd223human GRCh38 chr6: 73,118,474-73,446,748 , GRCh37.p13 chr6: 73,828,197-74,156,471 DPPA5, EIF3EP1, 15 more genes
    nsv6559734inversion1nstd223human GRCh38 chr6: 66,921,420-73,446,758 , GRCh37.p13 chr6: 67,631,313-74,156,481 RNA5SP208, KCNQ5, 72 more genes
    nsv6405055copy number variation1nstd223human GRCh38 chr6: 73,321,760-73,322,521 , GRCh37.p13 chr6: 74,031,483-74,032,244 SDCBP2P1
    nsv6401620copy number variation1nstd223human GRCh38 chr6: 73,321,913-73,327,191 , GRCh37.p13 chr6: 74,031,636-74,036,914 PAICSP3, SDCBP2P1
    nsv6401326copy number variation1nstd223human GRCh38 chr6: 73,275,286-73,325,685 , GRCh37.p13 chr6: 73,985,009-74,035,408 EIF3EP1, KHDC1, 3 more genes
    nsv6397601copy number variation1nstd223human GRCh38 chr6: 73,321,495-73,329,273 , GRCh37.p13 chr6: 74,031,218-74,038,996 SDCBP2P1, PAICSP3
    nsv6315402copy number variation1nstd102humanPathogenic GRCh37 chr6: 64,954,687-79,581,678 , GRCh38.p12 chr6: 64,244,794-78,871,961 LOC105377841, RPS6P8, 139 more genes
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6312591copy number variation1nstd102humanUncertain significance GRCh37 chr6: 73,879,449-74,210,458 , GRCh38.p12 chr6: 73,169,726-73,500,735 KCNQ5, DPPA5, 16 more genes
    nsv6291339copy number variation1nstd102humanPathogenic GRCh37 chr6: 70,165,296-79,920,769 , GRCh38.p12 chr6: 69,455,404-79,211,052 RNU6-84P, PGAM1P10, 113 more genes
    nsv6291322copy number variation1nstd102humanPathogenic GRCh37 chr6: 72,799,054-83,275,894 , GRCh38.p12 chr6: 72,089,351-82,566,177 RPS27P15, COX7A2, 118 more genes
    nsv6176017copy number variation1nstd214human GRCh38 chr6: 73,323,712-73,323,867 , GRCh37.p13 chr6: 74,033,435-74,033,590 SDCBP2P1
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