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Items: 1 to 20 of 62

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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 BORA, RNU6-71P, 1332 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 BORA, LOC105370271, 925 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 BORA, TEX30, 680 more genes
    nsv3907697copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,551,300-109,850,651 , GRCh38.p12 chr13: 52,977,165-109,198,303 BORA, GPC5, 565 more genes
    nsv3898603copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,457,841-91,796,698 , GRCh38.p12 chr13: 41,883,705-91,144,444 BORA, RNY4P30, 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 BORA, SRSF1P1, 541 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 BORA, RBM26, 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 BORA, RPL21P108, 539 more genes
    nsv3882264copy number variation1nstd102humanPathogenic GRCh38 chr13: 46,968,080-87,381,985 , GRCh37.p13 chr13: 47,542,215-88,034,240 BORA, ARL11, 428 more genes
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 BORA, RNU7-88P, 396 more genes
    nsv3895373copy number variation1nstd102humanPathogenic GRCh37 chr13: 57,058,434-94,684,615 , GRCh38.p12 chr13: 56,484,300-94,032,361 BORA, LINC00383, 359 more genes
    nsv3915859copy number variation1nstd102humanPathogenic GRCh38 chr13: 47,117,587-84,300,935 , GRCh37 chr13: 47,691,722-84,875,070 , NCBI36 chr13: 46,589,723-83,773,071 BORA, LOC105370231, 406 more genes
    nsv6291752copy number variation1nstd102humanPathogenic GRCh37 chr13: 59,574,760-89,410,027 , GRCh38.p12 chr13: 59,000,626-88,757,773 BORA, GYG1P2, 284 more genes
    nsv3913682copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,110,478-85,127,323 , NCBI36 chr13: 60,008,479-84,025,324 , GRCh38 chr13: 60,536,344-84,553,188 BORA, LOC105370251, 236 more genes
    nsv3902290copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,686,543-83,302,092 , GRCh38.p12 chr13: 61,112,409-82,727,957 BORA, LOC107987191, 216 more genes
    nsv3918305copy number variation1nstd102humanPathogenic GRCh37 chr13: 66,895,130-88,507,684 , GRCh38 chr13: 66,320,998-87,855,429 , NCBI36 chr13: 65,793,131-87,305,685 BORA, LINC00397, 208 more genes
    nsv3895213copy number variation1nstd102humanPathogenic GRCh37 chr13: 72,013,791-88,021,559 , GRCh38.p12 chr13: 71,439,659-87,369,304 BORA, MYCBP2, 157 more genes
    nsv3914942copy number variation1nstd102humanPathogenic NCBI36 chr13: 63,185,499-79,110,551 , GRCh37 chr13: 64,287,498-80,212,550 , GRCh38 chr13: 63,713,365-79,638,415 BORA, RIOK3P1, 175 more genes
    nsv4675244copy number variation1nstd102humanPathogenic GRCh37 chr13: 71,502,357-86,571,730 , GRCh38.p12 chr13: 70,928,225-85,997,595 BORA, RNU6-79P, 151 more genes
    nsv3902794copy number variation1nstd102humanPathogenic GRCh37 chr13: 72,174,742-82,221,361 , GRCh38.p12 chr13: 71,600,610-81,647,226 BORA, FABP5P1, 125 more genes
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