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Items: 1 to 20 of 36

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4674765copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,425,359-3,504,178 , GRCh38.p12 chr2: 3,421,588-3,500,407 , GRCh38.p12 chr2|NT_187522.1: 31,648-109,877 ADI1, TRAPPC12, 1 more genes
    nsv6290360copy number variation1nstd102humanUncertain significance GRCh37 chr2: 3,432,176-3,504,178 , GRCh38.p12 chr2: 3,428,405-3,500,407 , GRCh38.p12 chr2|NT_187522.1: 38,469-109,877 ADI1, TRAPPC12, 1 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 ADI1, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 ADI1, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 ADI1, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 ADI1, MTND2P22, 3724 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 ADI1, SLC35F6, 801 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 ADI1, ALLC, 674 more genes
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 ADI1, LOC105374455, 504 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 ADI1, LOC105373394, 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 ADI1, GTF3C2-AS1, 434 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 ADI1, LOC102723389, 362 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 ADI1, LOC105373359, 333 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 ADI1, EIF1P7, 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 ADI1, LOC100996549, 252 more genes
    nsv3886834copy number variation1nstd102humanPathogenic GRCh37 chr2: 12,770-20,081,474 , GRCh38.p12 chr2: 12,770-19,881,713 ADI1, LINC01249, 247 more genes
    nsv3908628copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,342-14,924,526 , GRCh37 chr2: 30,342-15,007,075 , GRCh38 chr2: 30,342-14,866,951 ADI1, RPS7, 198 more genes
    nsv3894966copy number variation1nstd102humanPathogenic NCBI36 chr2: 40,661-9,710,487 , GRCh38 chr2: 50,661-9,652,907 , GRCh37 chr2: 50,661-9,793,036 ADI1, PIK3CDP1, 120 more genes
    nsv4454966copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,770-7,502,796 , GRCh38.p12 chr2: 12,770-7,362,665 ADI1, LINC01810, 83 more genes
    nsv3903581copy number variation1nstd102humanPathogenic NCBI36 chr2: 20,341-4,957,824 , GRCh37 chr2: 30,341-4,979,949 , GRCh38 chr2: 30,341-4,932,359 ADI1, GAPDHP48, 52 more genes
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