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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    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
    nsv4606476copy number variation1nstd183human GRCh37 chr7: 64,264,741-64,568,852 , GRCh38.p12 chr7: 64,804,363-65,108,474 , ZNF138, 18 more genes
    nsv4525264copy number variation1nstd166human GRCh37.p13 chr7: 63,936,710-64,533,102 , GRCh38.p12 chr7: 64,476,332-65,072,724 , LOC441241, 30 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
    nsv4395646copy number variation1nstd174human GRCh37 chr7: 64,494,934-65,302,696 , GRCh38.p12 chr7: 65,034,556-65,837,709 , LOC84214, 22 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
    nsv4148716copy number variation1nstd166human GRCh37.p13 chr7: 64,472,000-64,573,000 , GRCh38.p12 chr7: 65,011,622-65,112,622 LOC441241, CCT6P3, 6 more genes
    nsv4148569copy number variation1nstd166human GRCh37.p13 chr7: 63,973,784-64,606,144 , GRCh38.p12 chr7: 64,513,406-65,145,766 , ERV3-1-ZNF117, 30 more genes
    nsv4134368copy number variation1nstd166human GRCh37.p13 chr7: 64,329,712-64,551,439 , GRCh38.p12 chr7: 64,869,334-65,091,061 , ERV3-1-ZNF117, 15 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
    nsv3923989copy number variation1nstd102humanLikely benign GRCh37 chr7: 64,499,811-65,012,082 , NCBI36 chr7: 64,137,246-64,708,360 , GRCh38 chr7: 65,039,433-65,606,012 SNORA22C, RSL24D1P3, 10 more genes
    nsv3923928copy number variation1nstd102humanLikely pathogenic NCBI36 chr7: 62,074,825-65,951,097 , GRCh37 chr7: 62,437,390-66,313,662 , GRCh38 chr7: 62,977,012-66,848,675 ASL, ERV3-1, 153 more genes
    nsv3923428copy number variation1nstd102humanPathogenic GRCh38 chr7: 64,657,050-72,243,063 , NCBI36 chr7: 63,754,863-71,345,984 , GRCh37 chr7: 64,117,428-71,708,048 LOC402279, LOC101929322, 112 more genes
    nsv3920837copy number variation1nstd102humanLikely benign GRCh37 chr7: 64,478,253-65,300,317 , NCBI36 chr7: 64,115,688-64,937,752 , GRCh38 chr7: 65,017,875-65,835,330 SNORA22, CCT6P3, 22 more genes
    nsv3919826copy number variation1nstd102humanPathogenic GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840 RNU6-438P, LOC105375300, 2682 more genes
    nsv3917682copy number variation1nstd102humanUncertain significance GRCh38 chr7: 64,879,046-65,086,621 , NCBI36 chr7: 63,976,859-64,184,434 , GRCh37 chr7: 64,339,424-64,546,999 CCT6P3, VN1R43P, 14 more genes
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