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Items: 1 to 20 of 441

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075087inversion1nstd229human GRCh38 chr13: 77,738,713-77,740,118 , GRCh37.p13 chr13: 78,312,848-78,314,253 SLAIN1
    nsv7065657inversion1nstd229human GRCh38 chr13: 76,225,150-84,243,039 , GRCh37.p13 chr13: 76,799,286-84,817,174 HSPD1P8, ELOCP23, 85 more genes
    nsv7061790inversion1nstd229human GRCh38 chr13: 76,348,646-84,254,120 , GRCh37.p13 chr13: 76,922,782-84,828,255 LINC01068, LOC105370264, 83 more genes
    nsv6947695copy number variation1nstd229human GRCh38 chr13: 77,757,762-78,362,648 , GRCh37.p13 chr13: 78,331,897-78,936,783 SRGNP1, EDNRB-AS1, 7 more genes
    nsv6946546copy number variation1nstd229human GRCh38 chr13: 77,749,155-77,749,750 , GRCh37.p13 chr13: 78,323,290-78,323,885 SLAIN1
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6493352copy number variation1nstd223human GRCh38 chr13: 77,730,801-77,733,700 , GRCh37.p13 chr13: 78,304,936-78,307,835 SLAIN1
    nsv6493096copy number variation1nstd223human GRCh38 chr13: 77,746,142-77,746,743 , GRCh37.p13 chr13: 78,320,277-78,320,878 SLAIN1
    nsv6492934copy number variation1nstd223human GRCh38 chr13: 77,756,955-77,757,348 , GRCh37.p13 chr13: 78,331,090-78,331,483 SLAIN1
    nsv6491887copy number variation1nstd223human GRCh38 chr13: 77,755,040-77,755,606 , GRCh37.p13 chr13: 78,329,175-78,329,741 SLAIN1
    nsv6490364copy number variation1nstd223human GRCh38 chr13: 77,725,179-77,725,804 , GRCh37.p13 chr13: 78,299,314-78,299,939 SLAIN1
    nsv6488978copy number variation1nstd223human GRCh38 chr13: 77,742,660-77,743,041 , GRCh37.p13 chr13: 78,316,795-78,317,176 SLAIN1
    nsv6488354copy number variation1nstd223human GRCh38 chr13: 77,750,093-77,832,716 , GRCh37.p13 chr13: 78,324,228-78,406,851 EDNRB-AS1, SLAIN1
    nsv6486736copy number variation1nstd223human GRCh38 chr13: 77,729,449-77,730,312 , GRCh37.p13 chr13: 78,303,584-78,304,447 SLAIN1
    nsv6480214copy number variation1nstd223human GRCh38 chr13: 77,727,114-77,727,506 , GRCh37.p13 chr13: 78,301,249-78,301,641 SLAIN1
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314172copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,574,661-87,784,831 , GRCh38.p12 chr13: 75,000,524-87,132,576 LMO7, TBC1D4, 119 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
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
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