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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112733copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,640,273-19,609,496 , GRCh38.p12 chr2: 15,500,149-19,409,735 LOC112267888, LOC105373454, 40 more genes
    nsv4728323copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,621,732-16,226,970 , GRCh38.p12 chr2: 15,481,608-16,086,848 GACAT3, RNU5E-7P, 9 more genes
    nsv4681098copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 15,744,252-17,675,820 , GRCh38.p12 chr2: 15,604,128-17,494,553 DDX1, MYCN, 17 more genes
    nsv4680259copy number variation1nstd189human GRCh37.p13 chr2: 15,812,492-16,105,132 , GRCh38.p12 chr2: 15,672,368-15,965,010 MYCN, MYCNOS, 5 more genes
    nsv4674356copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,478,363-17,062,394 , GRCh38.p12 chr2: 15,338,239-16,881,127 CYRIA, RNU5E-7P, 14 more genes
    nsv4519745copy number variation1nstd166human GRCh37.p13 chr2: 16,052,999-16,233,000 , GRCh38.p12 chr2: 15,912,876-16,092,878 GACAT3, MYCN, 3 more genes
    nsv4454513copy number variation1nstd102humanPathogenic GRCh37 chr2: 16,055,759-16,108,783 , GRCh38.p12 chr2: 15,915,636-15,968,661 MYCNUT, MYCNOS, 2 more genes
    nsv4451073copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,269,293-18,259,781 , GRCh38.p12 chr2: 12,129,167-18,078,515 LINC00276, TRIB2, 49 more genes
    nsv4451022copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,631,145-21,729,493 , GRCh38.p12 chr2: 15,491,021-21,506,621 RAD51AP2, LOC101928149, 82 more genes
    nsv3908896copy number variation1nstd102humanPathogenic GRCh37 chr2: 6,671,304-16,243,921 , GRCh38 chr2: 6,531,172-16,103,799 , NCBI36 chr2: 6,588,755-16,161,372 RNU6-1288P, MIR7515HG, 138 more genes
    nsv3908605copy number variation1nstd102humanPathogenic GRCh37 chr2: 66,097-55,797,773 , GRCh38 chr2: 66,097-55,570,637 , NCBI36 chr2: 56,097-55,651,277 SLC35F6, LOC105374458, 801 more genes
    nsv3908459copy number variation1nstd102humanPathogenic NCBI36 chr2: 1,647,394-23,740,517 , GRCh38 chr2: 1,664,615-23,664,142 , GRCh37 chr2: 1,668,387-23,887,012 EIF1P7, LOC105373398, 277 more genes
    nsv3908405copy number variation1nstd102humanPathogenic GRCh38 chr2: 17,019-20,001,056 , NCBI36 chr2: 7,019-20,064,298 , GRCh37 chr2: 17,019-20,200,817 LOC100996549, LOC105373479, 252 more genes
    nsv3908288copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,816-46,210,371 , GRCh38 chr2: 236,816-45,983,232 , NCBI36 chr2: 226,816-46,063,875 ALLC, LOC105373429, 674 more genes
    nsv3908038copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-33,936,576 , NCBI36 chr2: 2,770-33,790,080 , GRCh38 chr2: 12,770-33,711,509 LOC105373394, PGAM1P6, 507 more genes
    nsv3907033copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,341-28,496,035 , GRCh38 chr2: 30,341-28,419,664 , GRCh37 chr2: 30,341-28,642,531 GTF3C2-AS1, LOC105373399, 434 more genes
    nsv3903805copy number variation1nstd102humanBenign GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899 LOC101927723, SANBR, 1246 more genes
    nsv3900054copy number variation1nstd102humanPathogenic GRCh38 chr2: 13,664,310-16,228,425 , NCBI36 chr2: 13,721,886-16,273,174 , GRCh37 chr2: 13,804,435-16,409,693 RN7SL104P, LOC105373443, 16 more genes
    nsv3896997copy number variation1nstd102humanPathogenic GRCh38 chr2: 12,770-25,039,694 , GRCh37 chr2: 12,770-25,262,563 , NCBI36 chr2: 2,770-25,116,067 LOC105373359, MYT1L-AS1, 333 more genes
    nsv3893260copy number variation1nstd102humanPathogenic GRCh37 chr2: 17,019-26,541,714 , GRCh38 chr2: 17,019-26,318,846 , NCBI36 chr2: 7,019-26,395,218 LOC102723389, LOC105373433, 362 more genes
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