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Items: 1 to 20 of 22

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3910630copy number variation1nstd102humanPathogenic NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331 CHST10, DAZAP2P1, 2991 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CHST10, CYP1B1-AS1, 1649 more genes
    nsv3905242copy number variation1nstd102humanPathogenic NCBI36 chr2: 98,769,952-100,767,947 , GRCh38 chr2: 98,787,057-100,785,053 , GRCh37 chr2: 99,403,520-101,401,515 CHST10, LYG2, 30 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 CHST10, LOC112268439, 3737 more genes
    nsv3874648copy number variation1nstd102humanPathogenic GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305 CHST10, IGKV2OR2-10, 3737 more genes
    nsv3885544copy number variation1nstd102humanPathogenic GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609 CHST10, RNU6-674P, 3735 more genes
    nsv3882615copy number variation2nstd102humanPathogenic GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232 CHST10, MTND2P22, 3724 more genes
    nsv3876227copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,353,030-114,045,463 , GRCh38.p12 chr2: 95,687,282-113,287,886 CHST10, RNU4-8P, 346 more genes
    nsv3902899copy number variation1nstd102humanPathogenic NCBI36 chr2: 94,707,984-111,076,455 , GRCh38 chr2: 94,678,532-110,602,409 , GRCh37 chr2: 95,344,257-111,359,986 CHST10, MTCO3P45, 325 more genes
    nsv3877583copy number variation1nstd102humanPathogenic GRCh37 chr2: 95,529,039-108,518,266 , GRCh38.p12 chr2: 94,863,294-107,901,810 CHST10, RPL27AP4, 242 more genes
    nsv3907326copy number variation1nstd102humanPathogenic GRCh38 chr2: 97,672,522-110,211,318 , GRCh37 chr2: 98,288,985-110,968,895 , NCBI36 chr2: 97,655,417-110,326,184 CHST10, RPL22P11, 212 more genes
    nsv3906654copy number variation1nstd102humanPathogenic GRCh38 chr2: 91,443,218-102,334,856 , NCBI36 chr2: 90,981,410-102,317,748 , GRCh37 chr2: 91,617,683-102,951,316 CHST10, CHEK2P3, 197 more genes
    nsv3899291copy number variation1nstd102humanPathogenic GRCh37 chr2: 95,618,109-103,868,854 , GRCh38 chr2: 94,817,406-103,252,396 , NCBI36 chr2: 94,846,878-103,235,286 CHST10, IGKV2OR2-10, 178 more genes
    nsv3906499copy number variation1nstd102humanPathogenic NCBI36 chr2: 100,361,404-108,455,759 , GRCh37 chr2: 100,994,972-109,089,327 , GRCh38 chr2: 100,378,510-108,472,871 CHST10, LOC105373511, 132 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 CHST10, ACTG2, 1713 more genes
    nsv3895049copy number variation1nstd102humanLikely pathogenic NCBI36 chr2: 98,394,668-101,619,801 , GRCh37 chr2: 99,028,236-102,253,369 , GRCh38 chr2: 98,411,773-101,636,907 CHST10, INPP4A, 59 more genes
    nsv3890528copy number variation1nstd102humanLikely benign GRCh38 chr2: 100,404,604-100,908,738 , NCBI36 chr2: 100,387,498-100,891,632 , GRCh37 chr2: 101,021,066-101,525,200 CHST10, NMS, 12 more genes
    nsv3878618copy number variation1nstd102humanUncertain significance GRCh37 chr2: 100,890,121-101,188,008 , GRCh38.p12 chr2: 100,273,659-100,571,546 CHST10, RALBP1P2, 6 more genes
    nsv3879354copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,518,497-107,186,127 , GRCh38.p12 chr2: 94,852,752-106,569,671 CHST10, CD8B2, 231 more genes
    nsv3894524copy number variation1nstd102humanUncertain significance NCBI36 chr2: 99,236,392-101,542,533 , GRCh38 chr2: 99,253,497-101,559,639 , GRCh37 chr2: 99,869,960-102,176,101 CHST10, CREG2, 43 more genes
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