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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4453933copy number variation1nstd102humanPathogenic GRCh37 chr14: 60,975,886-60,976,919 , GRCh38 chr14: 60,509,168-60,510,201 SIX6
    nsv4729171copy number variation1nstd102humanUncertain significance GRCh37 chr14: 60,841,069-61,002,469 , GRCh38.p12 chr14: 60,374,351-60,535,751 SIX6, RMB8AP1, 3 more genes
    nsv3922652copy number variation1nstd102humanPathogenic GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231 SIX6, PARP1P2, 160 more genes
    nsv3923965copy number variation1nstd102humanPathogenic GRCh37 chr14: 60,383,769-67,217,521 , NCBI36 chr14: 59,453,522-66,287,274 , GRCh38 chr14: 59,917,051-66,750,803 SIX6, ESR2, 111 more genes
    nsv3924033copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,120,131-64,560,246 , GRCh38 chr14: 57,653,413-64,093,528 , NCBI36 chr14: 57,189,884-63,629,999 SIX6, DACT1, 105 more genes
    nsv3915521copy number variation1nstd102humanPathogenic NCBI36 chr14: 57,682,493-60,810,090 , GRCh37 chr14: 58,612,740-61,740,337 , GRCh38 chr14: 58,146,022-61,273,619 SIX6, DACT1, 61 more genes
    nsv3910126copy number variation1nstd102humanPathogenic NCBI36 chr14: 58,143,026-61,052,791 , GRCh37.p13 chr14: 59,073,273-61,983,038 , GRCh38.p12 chr14: 58,606,555-61,516,320 SIX6, AKR1B1P5, 45 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 SIX6, LOC440181, 1998 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 SIX6, BANF1P1, 1996 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 SIX6, LOC100289511, 1996 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 SIX6, DHRS7, 1946 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SIX6, SRMP2, 1929 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 SIX6, CRIP1, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 SIX6, MIR656, 1918 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 SIX6, PAPOLA-DT, 1338 more genes
    nsv6637682copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 57,804,997-63,590,203 , GRCh38.p12 chr14: 57,338,279-63,123,485 SIX6, PARP1P2, 91 more genes
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 SIX6, ACTN1, 400 more genes
    nsv7094439copy number variation2nstd102humanUncertain significance GRCh37 chr14: 60,976,117-61,447,691 , GRCh38.p12 chr14: 60,509,399-60,980,973 SIX6, MAD2L1P1, 12 more genes
    nsv5380830copy number variation1nstd102humanUncertain significance GRCh37 chr14: 60,976,117-61,191,013 , GRCh38.p12 chr14: 60,509,399-60,724,295 SIX6, MIR9718, 6 more genes
    nsv3898914copy number variation1nstd102humanUncertain significance GRCh37 chr14: 60,011,801-61,106,182 , GRCh38.p12 chr14: 59,545,083-60,639,464 SIX6, PPM1A, 20 more genes
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