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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3878152copy number variation1nstd102humanBenign GRCh37 chr1: 160,956,238-160,969,930 , GRCh38.p12 chr1: 160,986,448-161,000,140 F11R
    nsv3887879copy number variation1nstd102humanBenign GRCh37 chr1: 160,956,238-160,966,844 , GRCh38.p12 chr1: 160,986,448-160,997,054 F11R
    nsv3894131copy number variation1nstd102humanLikely benign GRCh37 chr13: 77,812,881-78,123,570 , GRCh38.p12 chr13: 77,238,746-77,549,435 LOC105370271, SCEL, 2 more genes
    nsv4456876copy number variation2nstd102humanUncertain significance GRCh37 chr5: 102,096,690-102,460,794 , GRCh38.p12 chr5: 102,760,986-103,125,090 PAM, GIN1, 3 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 PAM, MEGF10, 2080 more genes
    nsv3910270copy number variation1nstd102humanPathogenic GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141 RNU6-71P, LINC00676, 1332 more genes
    nsv3912840copy number variation1nstd102humanPathogenic NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643 CRB1, STX6, 1608 more genes
    nsv3924528copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908 LOC105370271, OR7E33P, 925 more genes
    nsv3884357copy number variation2nstd102humanPathogenic GRCh37 chr5: 86,400,000-154,000,000 , GRCh38.p12 chr5: 87,104,183-154,620,440 PAM, TXNDC15, 962 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv3907697copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,551,300-109,850,651 , GRCh38.p12 chr13: 52,977,165-109,198,303 GPC5, SNORD31B, 565 more genes
    nsv3898603copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,457,841-91,796,698 , GRCh38.p12 chr13: 41,883,705-91,144,444 RNY4P30, LOC107987191, 575 more genes
    nsv3918812copy number variation1nstd102humanPathogenic GRCh38 chr13: 44,967,523-92,738,168 , NCBI36 chr13: 44,439,658-92,188,422 , GRCh37 chr13: 45,541,658-93,390,421 SRSF1P1, LOC105370213, 541 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv3913649copy number variation1nstd102humanPathogenic GRCh38 chr13: 41,143,820-85,137,552 , GRCh37 chr13: 41,717,956-85,711,687 , NCBI36 chr13: 40,615,956-84,609,688 RPL21P108, LINC00330, 539 more genes
    nsv3882264copy number variation1nstd102humanPathogenic GRCh38 chr13: 46,968,080-87,381,985 , GRCh37.p13 chr13: 47,542,215-88,034,240 ARL11, RPL18P10, 428 more genes
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv3915450copy number variation1nstd102humanPathogenic GRCh37 chr5: 90,707,525-130,655,256 , NCBI36 chr5: 90,743,281-130,683,155 , GRCh38 chr5: 91,411,708-131,319,563 PAM, MCTP1, 422 more genes
    nsv3916468copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,670,423-127,412,115 , GRCh38 chr5: 90,374,606-128,076,423 , NCBI36 chr5: 89,706,179-127,440,014 PAM, LOC105379149, 406 more genes
    nsv3895373copy number variation1nstd102humanPathogenic GRCh37 chr13: 57,058,434-94,684,615 , GRCh38.p12 chr13: 56,484,300-94,032,361 LINC00383, LOC105370250, 359 more genes
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