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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144599copy number variation1nstd232human GRCh37.p13 chr13: 31,629,340-31,629,394 , GRCh38.p12 chr13: 31,055,203-31,055,257 LOC102723392
    nsv7094072copy number variation1nstd102humanUncertain significance GRCh37 chr13: 31,033,232-33,638,323 , GRCh38.p12 chr13: 30,459,095-33,064,186 N4BP2L2, RNY1P4, 37 more genes
    nsv7075032inversion1nstd229human GRCh38 chr13: 30,791,896-33,130,541 , GRCh37.p13 chr13: 31,366,033-33,704,678 BRCA2, TEX26, 31 more genes
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 more genes
    nsv7068176inversion1nstd229human GRCh38 chr13: 30,840,951-32,715,747 , GRCh37.p13 chr13: 31,415,088-33,289,884 MEDAG, N4BP2L1, 25 more genes
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6935495copy number variation1nstd229human GRCh38 chr13: 31,054,675-31,055,189 , GRCh37.p13 chr13: 31,628,812-31,629,326 LOC102723392
    nsv6933253copy number variation1nstd229human GRCh38 chr13: 31,054,343-31,065,216 , GRCh37.p13 chr13: 31,628,480-31,639,353 LOC102723392
    nsv6928860copy number variation1nstd229human GRCh38 chr13: 31,043,401-31,166,796 , GRCh37.p13 chr13: 31,617,538-31,740,933 WDR95P, LOC102723392, 2 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
    nsv6484994copy number variation1nstd223human GRCh38 chr13: 31,054,662-31,055,189 , GRCh37.p13 chr13: 31,628,799-31,629,326 LOC102723392
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 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
    nsv6291830copy number variation1nstd102humanUncertain significance GRCh38 chr13: 30,194,283-31,591,879 , GRCh37.p13 chr13: 30,768,420-32,166,016 LOC105370145, LINC00426, 26 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6204030copy number variation1nstd214human GRCh38 chr13: 31,054,218-31,054,386 , GRCh37.p13 chr13: 31,628,355-31,628,523 LOC102723392
    nsv6200079copy number variation1nstd214human GRCh38 chr13: 31,055,407-31,055,541 , GRCh37.p13 chr13: 31,629,544-31,629,678 LOC102723392
    nsv6187580copy number variation1nstd214human GRCh38 chr13: 31,055,203-31,055,257 , GRCh37.p13 chr13: 31,629,340-31,629,394 LOC102723392
    nsv6132755copy number variation1nstd213human GRCh37 chr13: 31,340,000-31,830,001 , GRCh38.p12 chr13: 30,765,863-31,255,864 HSPH1, MEDAG, 9 more genes
    nsv6132639copy number variation1nstd213human GRCh37 chr13: 31,460,000-31,710,001 , GRCh38.p12 chr13: 30,885,863-31,135,864 HSPH1, MEDAG, 5 more genes
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