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nsv7098702

  • Variant Calls:24
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):187,411,365-187,411,365Question Mark
    Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):187,411,390-187,411,390Question Mark
    Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):187,411,390-187,411,390Question Mark
    Overlapping variant regions from other studies: 184 SVs from 34 studies. See in: genome view    
    Remapped(Score: Perfect):187,970,370-187,970,370Question Mark
    Overlapping variant regions from other studies: 136 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):219,493,768-219,493,768Question Mark
    Overlapping variant regions from other studies: 136 SVs from 23 studies. See in: genome view    
    Remapped(Score: Perfect):219,493,768-219,493,768Question Mark
    Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):130,632,936-130,632,936Question Mark
    Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):130,632,938-130,632,938Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):132,183,236-132,183,236Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):132,183,240-132,183,240Question Mark
    Overlapping variant regions from other studies: 96 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):136,709,532-136,709,532Question Mark
    Overlapping variant regions from other studies: 96 SVs from 15 studies. See in: genome view    
    Remapped(Score: Perfect):136,709,532-136,709,532Question Mark
    Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):136,737,018-136,737,018Question Mark
    Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):136,737,022-136,737,022Question Mark
    Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):136,737,949-136,737,949Question Mark
    Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
    Remapped(Score: Perfect):136,737,951-136,737,951Question Mark
    Overlapping variant regions from other studies: 162 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):111,970,982-111,970,982Question Mark
    Overlapping variant regions from other studies: 99 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):114,122,054-114,122,054Question Mark
    Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):114,566,197-114,566,197Question Mark
    Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):114,566,198-114,566,198Question Mark
    Overlapping variant regions from other studies: 152 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):23,453,068-23,453,068Question Mark
    Overlapping variant regions from other studies: 152 SVs from 28 studies. See in: genome view    
    Remapped(Score: Perfect):23,453,072-23,453,072Question Mark
    Overlapping variant regions from other studies: 149 SVs from 24 studies. See in: genome view    
    Remapped(Score: Perfect):23,472,609-23,472,609Question Mark
    Overlapping variant regions from other studies: 156 SVs from 26 studies. See in: genome view    
    Remapped(Score: Perfect):23,641,670-23,641,670Question Mark
    Overlapping variant regions from other studies: 152 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):102,396,658-102,396,658Question Mark
    Overlapping variant regions from other studies: 152 SVs from 12 studies. See in: genome view    
    Remapped(Score: Perfect):102,396,662-102,396,662Question Mark
    Overlapping variant regions from other studies: 194 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):104,845,779-104,845,779Question Mark
    Overlapping variant regions from other studies: 194 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):104,845,780-104,845,780Question Mark
    Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):29,670,675-29,670,675Question Mark
    Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):29,670,678-29,670,678Question Mark
    Overlapping variant regions from other studies: 110 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):34,700,641-34,700,641Question Mark
    Overlapping variant regions from other studies: 110 SVs from 22 studies. See in: genome view    
    Remapped(Score: Perfect):34,700,642-34,700,642Question Mark
    Overlapping variant regions from other studies: 131 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):35,208,085-35,208,085Question Mark
    Overlapping variant regions from other studies: 131 SVs from 25 studies. See in: genome view    
    Remapped(Score: Perfect):35,208,090-35,208,090Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):37,971,667-37,971,667Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Remapped(Score: Perfect):37,971,739-37,971,739Question Mark
    Overlapping variant regions from other studies: 166 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):59,313,959-59,313,959Question Mark
    Overlapping variant regions from other studies: 166 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):59,313,962-59,313,962Question Mark
    Overlapping variant regions from other studies: 187 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):65,927,743-65,927,743Question Mark
    Overlapping variant regions from other studies: 187 SVs from 21 studies. See in: genome view    
    Remapped(Score: Perfect):65,927,743-65,927,743Question Mark
    Overlapping variant regions from other studies: 219 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):66,855,473-66,855,473Question Mark
    Overlapping variant regions from other studies: 219 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):66,855,479-66,855,479Question Mark
    Overlapping variant regions from other studies: 162 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):73,975,574-73,975,574Question Mark
    Overlapping variant regions from other studies: 162 SVs from 17 studies. See in: genome view    
    Remapped(Score: Perfect):73,975,574-73,975,574Question Mark
    Overlapping variant regions from other studies: 154 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):75,880,105-75,880,105Question Mark
    Overlapping variant regions from other studies: 154 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):75,880,107-75,880,107Question Mark
    Overlapping variant regions from other studies: 183 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):90,571,751-90,571,751Question Mark
    Overlapping variant regions from other studies: 183 SVs from 19 studies. See in: genome view    
    Remapped(Score: Perfect):90,571,755-90,571,755Question Mark
    Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
    Submitted genomic187,380,497-187,380,497Question Mark
    Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
    Submitted genomic187,380,522-187,380,522Question Mark
    Overlapping variant regions from other studies: 158 SVs from 24 studies. See in: genome view    
    Submitted genomic187,380,522-187,380,522Question Mark
    Overlapping variant regions from other studies: 184 SVs from 34 studies. See in: genome view    
    Submitted genomic187,939,501-187,939,501Question Mark
    Overlapping variant regions from other studies: 140 SVs from 23 studies. See in: genome view    
    Submitted genomic219,667,110-219,667,110Question Mark
    Overlapping variant regions from other studies: 140 SVs from 23 studies. See in: genome view    
    Submitted genomic219,667,110-219,667,110Question Mark
    Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view    
    Submitted genomic130,954,081-130,954,081Question Mark
    Overlapping variant regions from other studies: 93 SVs from 19 studies. See in: genome view    
    Submitted genomic130,954,083-130,954,083Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Submitted genomic132,504,376-132,504,376Question Mark
    Overlapping variant regions from other studies: 99 SVs from 22 studies. See in: genome view    
    Submitted genomic132,504,380-132,504,380Question Mark
    Overlapping variant regions from other studies: 96 SVs from 15 studies. See in: genome view    
    Submitted genomic137,030,670-137,030,670Question Mark
    Overlapping variant regions from other studies: 96 SVs from 15 studies. See in: genome view    
    Submitted genomic137,030,670-137,030,670Question Mark
    Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
    Submitted genomic137,058,156-137,058,156Question Mark
    Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
    Submitted genomic137,058,160-137,058,160Question Mark
    Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
    Submitted genomic137,059,087-137,059,087Question Mark
    Overlapping variant regions from other studies: 92 SVs from 13 studies. See in: genome view    
    Submitted genomic137,059,089-137,059,089Question Mark
    Overlapping variant regions from other studies: 162 SVs from 30 studies. See in: genome view    
    Submitted genomic111,611,037-111,611,037Question Mark
    Overlapping variant regions from other studies: 99 SVs from 21 studies. See in: genome view    
    Submitted genomic113,762,109-113,762,109Question Mark
    Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view    
    Submitted genomic117,328,477-117,328,477Question Mark
    Overlapping variant regions from other studies: 132 SVs from 28 studies. See in: genome view    
    Submitted genomic117,328,478-117,328,478Question Mark
    Overlapping variant regions from other studies: 152 SVs from 28 studies. See in: genome view    
    Submitted genomic23,606,002-23,606,002Question Mark
    Overlapping variant regions from other studies: 152 SVs from 28 studies. See in: genome view    
    Submitted genomic23,606,006-23,606,006Question Mark
    Overlapping variant regions from other studies: 149 SVs from 24 studies. See in: genome view    
    Submitted genomic23,625,543-23,625,543Question Mark
    Overlapping variant regions from other studies: 156 SVs from 26 studies. See in: genome view    
    Submitted genomic23,794,604-23,794,604Question Mark
    Overlapping variant regions from other studies: 152 SVs from 12 studies. See in: genome view    
    Submitted genomic103,049,008-103,049,008Question Mark
    Overlapping variant regions from other studies: 152 SVs from 12 studies. See in: genome view    
    Submitted genomic103,049,012-103,049,012Question Mark
    Overlapping variant regions from other studies: 194 SVs from 21 studies. See in: genome view    
    Submitted genomic105,498,130-105,498,130Question Mark
    Overlapping variant regions from other studies: 194 SVs from 21 studies. See in: genome view    
    Submitted genomic105,498,131-105,498,131Question Mark
    Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
    Submitted genomic30,244,812-30,244,812Question Mark
    Overlapping variant regions from other studies: 87 SVs from 18 studies. See in: genome view    
    Submitted genomic30,244,815-30,244,815Question Mark
    Overlapping variant regions from other studies: 110 SVs from 22 studies. See in: genome view    
    Submitted genomic35,274,778-35,274,778Question Mark
    Overlapping variant regions from other studies: 110 SVs from 22 studies. See in: genome view    
    Submitted genomic35,274,779-35,274,779Question Mark
    Overlapping variant regions from other studies: 131 SVs from 25 studies. See in: genome view    
    Submitted genomic35,782,222-35,782,222Question Mark
    Overlapping variant regions from other studies: 131 SVs from 25 studies. See in: genome view    
    Submitted genomic35,782,227-35,782,227Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Submitted genomic38,545,804-38,545,804Question Mark
    Overlapping variant regions from other studies: 113 SVs from 18 studies. See in: genome view    
    Submitted genomic38,545,876-38,545,876Question Mark
    Overlapping variant regions from other studies: 166 SVs from 17 studies. See in: genome view    
    Submitted genomic59,888,093-59,888,093Question Mark
    Overlapping variant regions from other studies: 166 SVs from 17 studies. See in: genome view    
    Submitted genomic59,888,096-59,888,096Question Mark
    Overlapping variant regions from other studies: 187 SVs from 21 studies. See in: genome view    
    Submitted genomic66,501,875-66,501,875Question Mark
    Overlapping variant regions from other studies: 187 SVs from 21 studies. See in: genome view    
    Submitted genomic66,501,875-66,501,875Question Mark
    Overlapping variant regions from other studies: 219 SVs from 27 studies. See in: genome view    
    Submitted genomic67,429,605-67,429,605Question Mark
    Overlapping variant regions from other studies: 219 SVs from 27 studies. See in: genome view    
    Submitted genomic67,429,611-67,429,611Question Mark
    Overlapping variant regions from other studies: 162 SVs from 17 studies. See in: genome view    
    Submitted genomic74,549,711-74,549,711Question Mark
    Overlapping variant regions from other studies: 162 SVs from 17 studies. See in: genome view    
    Submitted genomic74,549,711-74,549,711Question Mark
    Overlapping variant regions from other studies: 154 SVs from 19 studies. See in: genome view    
    Submitted genomic76,454,241-76,454,241Question Mark
    Overlapping variant regions from other studies: 154 SVs from 19 studies. See in: genome view    
    Submitted genomic76,454,243-76,454,243Question Mark
    Overlapping variant regions from other studies: 183 SVs from 19 studies. See in: genome view    
    Submitted genomic91,224,005-91,224,005Question Mark
    Overlapping variant regions from other studies: 183 SVs from 19 studies. See in: genome view    
    Submitted genomic91,224,009-91,224,009Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1187,411,365187,411,365+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1187,411,390187,411,390+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1187,411,390187,411,390+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1187,970,370187,970,370-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1219,493,768219,493,768+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1219,493,768219,493,768-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6130,632,936130,632,936-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6130,632,938130,632,938+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6132,183,236132,183,236+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6132,183,240132,183,240-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6136,709,532136,709,532+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6136,709,532136,709,532-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6136,737,018136,737,018+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6136,737,022136,737,022-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6136,737,949136,737,949-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6136,737,951136,737,951+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7111,970,982111,970,982+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7114,122,054114,122,054-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9114,566,197114,566,197-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9114,566,198114,566,198+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1223,453,06823,453,068-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1223,453,07223,453,072+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1223,472,60923,472,609+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1223,641,67023,641,670-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr13102,396,658102,396,658-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr13102,396,662102,396,662+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr13104,845,779104,845,779-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr13104,845,780104,845,780+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1329,670,67529,670,675+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1329,670,67829,670,678-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1334,700,64134,700,641-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1334,700,64234,700,642+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1335,208,08535,208,085-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1335,208,09035,208,090+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1337,971,66737,971,667+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1337,971,73937,971,739-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1359,313,95959,313,959+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1359,313,96259,313,962-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1365,927,74365,927,743+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1365,927,74365,927,743-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1366,855,47366,855,473+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1366,855,47966,855,479+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1373,975,57473,975,574+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1373,975,57473,975,574-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1375,880,10575,880,105+
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1375,880,10775,880,107-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1390,571,75190,571,751-
    nsv7098702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000013.11Chr1390,571,75590,571,755+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1187,380,497187,380,497+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1187,380,522187,380,522+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1187,380,522187,380,522+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1187,939,501187,939,501-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1219,667,110219,667,110+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000001.10Chr1219,667,110219,667,110-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6130,954,081130,954,081-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6130,954,083130,954,083+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6132,504,376132,504,376+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6132,504,380132,504,380-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6137,030,670137,030,670+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6137,030,670137,030,670-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6137,058,156137,058,156+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6137,058,160137,058,160-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6137,059,087137,059,087-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000006.11Chr6137,059,089137,059,089+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7111,611,037111,611,037+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7113,762,109113,762,109-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr9117,328,477117,328,477-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr9117,328,478117,328,478+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1223,606,00223,606,002-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1223,606,00623,606,006+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1223,625,54323,625,543+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1223,794,60423,794,604-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr13103,049,008103,049,008-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr13103,049,012103,049,012+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr13105,498,130105,498,130-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr13105,498,131105,498,131+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1330,244,81230,244,812+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1330,244,81530,244,815-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1335,274,77835,274,778-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1335,274,77935,274,779+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1335,782,22235,782,222-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1335,782,22735,782,227+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1338,545,80438,545,804+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1338,545,87638,545,876-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1359,888,09359,888,093+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1359,888,09659,888,096-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1366,501,87566,501,875+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1366,501,87566,501,875-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1367,429,60567,429,605+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1367,429,61167,429,611+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1374,549,71174,549,711+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1374,549,71174,549,711-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1376,454,24176,454,241+
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1376,454,24376,454,243-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1391,224,00591,224,005-
    nsv7098702Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000013.10Chr1391,224,00991,224,009+

    Variant Call Information

    Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
    nssv18792525intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792524interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792529interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792526interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792528interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792539interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792518intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792538intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792535interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792536intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792537intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792519interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792541interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792523interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792521interchromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792534intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792533intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792540intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792530intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792532intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792531intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792520intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792527intrachromosomal translocationFHU20-098SequencingSequence alignment24
    nssv18792522intrachromosomal translocationFHU20-098SequencingSequence alignment24

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
    nssv18792525RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1187,411,365187,411,365+
    nssv18792524RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1187,411,390187,411,390+
    nssv18792525RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1187,411,390187,411,390+
    nssv18792529RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1187,970,370187,970,370-
    nssv18792526RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1219,493,768219,493,768-
    nssv18792528RemappedPerfectGRCh38.p12First PassNC_000001.11Chr1219,493,768219,493,768+
    nssv18792539RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6130,632,936130,632,936-
    nssv18792518RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6130,632,938130,632,938+
    nssv18792538RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6132,183,236132,183,236+
    nssv18792535RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6132,183,240132,183,240-
    nssv18792536RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6136,709,532136,709,532+
    nssv18792537RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6136,709,532136,709,532-
    nssv18792538RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6136,737,018136,737,018+
    nssv18792537RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6136,737,022136,737,022-
    nssv18792518RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6136,737,949136,737,949-
    nssv18792536RemappedPerfectGRCh38.p12First PassNC_000006.12Chr6136,737,951136,737,951+
    nssv18792519RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7111,970,982111,970,982+
    nssv18792541RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7114,122,054114,122,054-
    nssv18792523RemappedPerfectGRCh38.p12First PassNC_000009.12Chr9114,566,197114,566,197-
    nssv18792521RemappedPerfectGRCh38.p12First PassNC_000009.12Chr9114,566,198114,566,198+
    nssv18792535RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1223,453,06823,453,068-
    nssv18792534RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1223,453,07223,453,072+
    nssv18792534RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1223,472,60923,472,609+
    nssv18792539RemappedPerfectGRCh38.p12First PassNC_000012.12Chr1223,641,67023,641,670-
    nssv18792533RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1329,670,67529,670,675+
    nssv18792540RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1329,670,67829,670,678-
    nssv18792530RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1334,700,64134,700,641-
    nssv18792532RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1334,700,64234,700,642+
    nssv18792532RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1335,208,08535,208,085-
    nssv18792531RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1335,208,09035,208,090+
    nssv18792531RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1337,971,66737,971,667+
    nssv18792520RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1337,971,73937,971,739-
    nssv18792519RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1359,313,95959,313,959+
    nssv18792520RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1359,313,96259,313,962-
    nssv18792527RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1365,927,74365,927,743+
    nssv18792530RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1365,927,74365,927,743-
    nssv18792529RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1366,855,47366,855,473+
    nssv18792524RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1366,855,47966,855,479+
    nssv18792526RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1373,975,57473,975,574+
    nssv18792527RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1373,975,57473,975,574-
    nssv18792528RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1375,880,10575,880,105+
    nssv18792522RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1375,880,10775,880,107-
    nssv18792522RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1390,571,75190,571,751-
    nssv18792521RemappedPerfectGRCh38.p12First PassNC_000013.11Chr1390,571,75590,571,755+
    nssv18792541RemappedPerfectGRCh38.p12First PassNC_000013.11Chr13102,396,658102,396,658-
    nssv18792523RemappedPerfectGRCh38.p12First PassNC_000013.11Chr13102,396,662102,396,662+
    nssv18792540RemappedPerfectGRCh38.p12First PassNC_000013.11Chr13104,845,779104,845,779-
    nssv18792533RemappedPerfectGRCh38.p12First PassNC_000013.11Chr13104,845,780104,845,780+
    nssv18792525Submitted genomicGRCh37 (hg19)NC_000001.10Chr1187,380,497187,380,497+
    nssv18792524Submitted genomicGRCh37 (hg19)NC_000001.10Chr1187,380,522187,380,522+
    nssv18792525Submitted genomicGRCh37 (hg19)NC_000001.10Chr1187,380,522187,380,522+
    nssv18792529Submitted genomicGRCh37 (hg19)NC_000001.10Chr1187,939,501187,939,501-
    nssv18792526Submitted genomicGRCh37 (hg19)NC_000001.10Chr1219,667,110219,667,110-
    nssv18792528Submitted genomicGRCh37 (hg19)NC_000001.10Chr1219,667,110219,667,110+
    nssv18792539Submitted genomicGRCh37 (hg19)NC_000006.11Chr6130,954,081130,954,081-
    nssv18792518Submitted genomicGRCh37 (hg19)NC_000006.11Chr6130,954,083130,954,083+
    nssv18792538Submitted genomicGRCh37 (hg19)NC_000006.11Chr6132,504,376132,504,376+
    nssv18792535Submitted genomicGRCh37 (hg19)NC_000006.11Chr6132,504,380132,504,380-
    nssv18792536Submitted genomicGRCh37 (hg19)NC_000006.11Chr6137,030,670137,030,670+
    nssv18792537Submitted genomicGRCh37 (hg19)NC_000006.11Chr6137,030,670137,030,670-
    nssv18792538Submitted genomicGRCh37 (hg19)NC_000006.11Chr6137,058,156137,058,156+
    nssv18792537Submitted genomicGRCh37 (hg19)NC_000006.11Chr6137,058,160137,058,160-
    nssv18792518Submitted genomicGRCh37 (hg19)NC_000006.11Chr6137,059,087137,059,087-
    nssv18792536Submitted genomicGRCh37 (hg19)NC_000006.11Chr6137,059,089137,059,089+
    nssv18792519Submitted genomicGRCh37 (hg19)NC_000007.13Chr7111,611,037111,611,037+
    nssv18792541Submitted genomicGRCh37 (hg19)NC_000007.13Chr7113,762,109113,762,109-
    nssv18792523Submitted genomicGRCh37 (hg19)NC_000009.11Chr9117,328,477117,328,477-
    nssv18792521Submitted genomicGRCh37 (hg19)NC_000009.11Chr9117,328,478117,328,478+
    nssv18792535Submitted genomicGRCh37 (hg19)NC_000012.11Chr1223,606,00223,606,002-
    nssv18792534Submitted genomicGRCh37 (hg19)NC_000012.11Chr1223,606,00623,606,006+
    nssv18792534Submitted genomicGRCh37 (hg19)NC_000012.11Chr1223,625,54323,625,543+
    nssv18792539Submitted genomicGRCh37 (hg19)NC_000012.11Chr1223,794,60423,794,604-
    nssv18792533Submitted genomicGRCh37 (hg19)NC_000013.10Chr1330,244,81230,244,812+
    nssv18792540Submitted genomicGRCh37 (hg19)NC_000013.10Chr1330,244,81530,244,815-
    nssv18792530Submitted genomicGRCh37 (hg19)NC_000013.10Chr1335,274,77835,274,778-
    nssv18792532Submitted genomicGRCh37 (hg19)NC_000013.10Chr1335,274,77935,274,779+
    nssv18792532Submitted genomicGRCh37 (hg19)NC_000013.10Chr1335,782,22235,782,222-
    nssv18792531Submitted genomicGRCh37 (hg19)NC_000013.10Chr1335,782,22735,782,227+
    nssv18792531Submitted genomicGRCh37 (hg19)NC_000013.10Chr1338,545,80438,545,804+
    nssv18792520Submitted genomicGRCh37 (hg19)NC_000013.10Chr1338,545,87638,545,876-
    nssv18792519Submitted genomicGRCh37 (hg19)NC_000013.10Chr1359,888,09359,888,093+
    nssv18792520Submitted genomicGRCh37 (hg19)NC_000013.10Chr1359,888,09659,888,096-
    nssv18792527Submitted genomicGRCh37 (hg19)NC_000013.10Chr1366,501,87566,501,875+
    nssv18792530Submitted genomicGRCh37 (hg19)NC_000013.10Chr1366,501,87566,501,875-
    nssv18792529Submitted genomicGRCh37 (hg19)NC_000013.10Chr1367,429,60567,429,605+
    nssv18792524Submitted genomicGRCh37 (hg19)NC_000013.10Chr1367,429,61167,429,611+
    nssv18792526Submitted genomicGRCh37 (hg19)NC_000013.10Chr1374,549,71174,549,711+
    nssv18792527Submitted genomicGRCh37 (hg19)NC_000013.10Chr1374,549,71174,549,711-
    nssv18792528Submitted genomicGRCh37 (hg19)NC_000013.10Chr1376,454,24176,454,241+
    nssv18792522Submitted genomicGRCh37 (hg19)NC_000013.10Chr1376,454,24376,454,243-
    nssv18792522Submitted genomicGRCh37 (hg19)NC_000013.10Chr1391,224,00591,224,005-
    nssv18792521Submitted genomicGRCh37 (hg19)NC_000013.10Chr1391,224,00991,224,009+
    nssv18792541Submitted genomicGRCh37 (hg19)NC_000013.10Chr13103,049,008103,049,008-
    nssv18792523Submitted genomicGRCh37 (hg19)NC_000013.10Chr13103,049,012103,049,012+
    nssv18792540Submitted genomicGRCh37 (hg19)NC_000013.10Chr13105,498,130105,498,130-
    nssv18792533Submitted genomicGRCh37 (hg19)NC_000013.10Chr13105,498,131105,498,131+

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    No genotype data were submitted for this variant

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