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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927170copy number variation1nstd209human GRCh38 chr7: 64,022,336-64,278,876 , GRCh37.p13 chr7: 63,482,714-63,739,254 LOC105375317, ZNF735, 21 more genes
    nsv5926373copy number variation1nstd209human GRCh38 chr7: 64,063,525-64,329,680 , GRCh37.p13 chr7: 63,523,903-63,790,058 VN1R38P, SAPCD2P1, 21 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5109019mobile element insertion1nstd203human GRCh38 chr7: 64,180,706-64,180,719 , GRCh37.p13 chr7: 63,641,084-63,641,097 VN1R38P, SAPCD2P1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4761040inversion1nstd199human GRCh37 chr7: 55,830,732-65,288,125 , GRCh38.p12 chr7: 55,763,039-65,823,138 , CCT6A, 247 more genes
    nsv4729639copy number variation1nstd102humanUncertain significance GRCh37 chr7: 62,508,852-64,940,346 , GRCh38.p12 chr7: 63,048,474-65,475,433 VN1R39P, LOC105375324, 113 more genes
    nsv4728981copy number variation1nstd102humanUncertain significance GRCh37 chr7: 62,495,083-64,927,758 , GRCh38.p12 chr7: 63,034,705-65,462,845 LOC105375321, GUSBP6, 113 more genes
    nsv4608921copy number variation1nstd183human GRCh37 chr7: 63,448,096-64,413,552 , GRCh38.p12 chr7: 63,987,718-64,953,174 , VN1R41P, 52 more genes
    nsv4606786copy number variation1nstd183human GRCh37 chr7: 62,520,372-64,227,496 , GRCh38.p12 chr7: 63,059,994-64,767,118 , LOC105375326, 89 more genes
    nsv4598888copy number variation2nstd183human GRCh37 chr7: 63,370,292-63,847,365 , GRCh38.p12 chr7: 63,909,914-64,386,987 LOC105375322, MTND3P2, 35 more genes
    nsv4524365copy number variation1nstd166human GRCh37.p13 chr7: 63,523,999-63,790,000 , GRCh38.p12 chr7: 64,063,621-64,329,622 VN1R37P, ZNF679, 21 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4399125copy number variation1nstd174human GRCh37 chr7: 63,482,832-63,739,372 , GRCh38.p12 chr7: 64,022,454-64,278,994 GUSBP6, VN1R39P, 21 more genes
    nsv4394661copy number variation1nstd174human GRCh37 chr7: 63,520,745-63,903,255 , GRCh38.p12 chr7: 64,060,367-64,442,877 MTATP6P18, ZNF735, 26 more genes
    nsv4386668copy number variation1nstd173human GRCh37 chr7: 63,530,076-63,796,210 , GRCh38.p12 chr7: 64,069,698-64,335,832 VN1R39P, MTND4P2, 21 more genes
    nsv4373059copy number variation1nstd173human GRCh37 chr7: 63,530,076-63,784,894 , GRCh38.p12 chr7: 64,069,698-64,324,516 LOC105375322, LOC105375319, 21 more genes
    nsv4352523inversion1nstd102humanPathogenic GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550 ACHE, ADCY1, 1532 more genes
    nsv4140164copy number variation1nstd166human GRCh37.p13 chr7: 63,352,508-63,858,518 , GRCh38.p12 chr7: 63,892,130-64,398,140 MTND3P2, VN1R37P, 36 more genes
    nsv4132870copy number variation1nstd166human GRCh37.p13 chr7: 62,491,653-64,942,895 , GRCh38.p12 chr7: 63,031,275-65,477,982 , GUSBP6, 117 more genes
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