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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068863inversion1nstd229human GRCh38 chr13: 27,564,614-31,455,391 , GRCh37.p13 chr13: 28,138,751-32,029,528 MFAP1P1, RN7SL272P, 70 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
    nsv6918657copy number variation1nstd229human GRCh38 chr13: 30,367,401-30,509,500 , GRCh37.p13 chr13: 30,941,538-31,083,637 LINC00426, HMGB1, 3 more genes
    nsv6918120copy number variation1nstd229human GRCh38 chr13: 30,389,860-30,459,944 , GRCh37.p13 chr13: 30,963,997-31,034,081 HMGB1, LINC01058, 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
    nsv6487758copy number variation1nstd223human GRCh38 chr13: 30,445,165-30,448,096 , GRCh37.p13 chr13: 31,019,302-31,022,233 LOC107984577
    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
    nsv6289845copy number variation1nstd102humanUncertain significance GRCh37 chr13: 31,009,874-31,269,950 , GRCh38.p12 chr13: 30,435,737-30,695,813 PTPN2P2, TRN-GTT2-4, 5 more genes
    nsv6137701copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 28,669,064-31,367,407 , GRCh38.p12 chr13: 28,094,927-30,793,270 ALOX5AP, FLT1, 41 more genes
    nsv6132543copy number variation1nstd213human GRCh37 chr13: 19,020,000-67,280,001 , GRCh38.p12 chr13: 18,445,862-66,705,869 , PARP4, 770 more genes
    nsv6132475copy number variation1nstd213human GRCh37 chr13: 26,620,000-32,650,001 , GRCh38.p12 chr13: 26,045,862-32,075,864 ALOX5AP, HMGB1, 106 more genes
    nsv6112810copy number variation1nstd102humanPathogenic GRCh37 chr13: 28,925,153-34,061,696 , GRCh38.p12 chr13: 28,351,016-33,487,559 MTUS2, ALOX5AP, 70 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5504637copy number variation1nstd206human GRCh38 chr13: 30,413,089-30,445,183 , GRCh37.p13 chr13: 30,987,226-31,019,320 LOC107984577, UBE2L5, 1 more genes
    nsv5500967copy number variation1nstd206human GRCh38 chr13: 30,445,166-30,448,123 , GRCh37.p13 chr13: 31,019,303-31,022,260 LOC107984577
    nsv5145519mobile element insertion1nstd203human GRCh38 chr13: 30,447,343-30,447,362 , GRCh37.p13 chr13: 31,021,480-31,021,499 LOC107984577
    nsv4996786copy number variation1nstd200human GRCh38 chr13: 30,445,140-30,448,110 , GRCh37.p13 chr13: 31,019,277-31,022,247 LOC107984577
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