U.S. flag

An official website of the United States government

nsv4386088

  • Variant Calls:74
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:36,484

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 975 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):11,067,331-11,103,814Question Mark
Overlapping variant regions from other studies: 976 SVs from 85 studies. See in: genome view    
Submitted genomic11,219,930-11,256,413Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4386088RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1211,067,33111,103,814
nsv4386088Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000012.11Chr1211,219,93011,256,413

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15612880copy number loss1-0675-003SNP arrayGenotyping25
nssv15613239copy number loss1-0680-003SNP arrayGenotyping24
nssv15620788copy number loss1-1003-003SNP arrayGenotyping15
nssv15624817copy number loss1-0403-004SNP arrayGenotyping32
nssv15624976copy number loss1-0340-004SNP arrayGenotyping20
nssv15626952copy number loss1-0458-002SNP arrayGenotyping20
nssv15627386copy number loss1-0539-002SNP arrayGenotyping22
nssv15627469copy number loss1-0483-002SNP arrayGenotyping13
nssv15627583copy number loss1-0489-004SNP arrayGenotyping18
nssv15629308copy number loss1-0541-002SNP arrayGenotyping17
nssv15629358copy number loss1-0541-005SNP arrayGenotyping17
nssv15629733copy number loss1-0574-003SNP arrayGenotyping16
nssv15630290copy number loss1-0600-003SNP arrayGenotyping25
nssv15631645copy number loss10-0003-003SNP arrayGenotyping22
nssv15632056copy number loss10-0009-002SNP arrayGenotyping21
nssv15632257copy number loss10-1095-004SNP arrayGenotyping25
nssv15632834copy number loss10-0009-003SNP arrayGenotyping25
nssv15635644copy number loss11-0050-003SNP arrayGenotyping16
nssv15639264copy number loss14-0284-003SNP arrayGenotyping25
nssv15640872copy number loss14-0312-002SNP arrayGenotyping29
nssv15643540copy number gain16-1013-003SNP arrayGenotyping14
nssv15645229copy number loss2-0126-002SNP arrayGenotyping16
nssv15645813copy number loss2-0197-002SNP arrayGenotyping17
nssv15646263copy number loss2-0018-002SNP arrayGenotyping20
nssv15646284copy number loss2-0018-003SNP arrayGenotyping23
nssv15646650copy number loss2-1272-003SNP arrayGenotyping15
nssv15647224copy number loss2-1085-003SNP arrayGenotyping16
nssv15647429copy number loss2-1244-003SNP arrayGenotyping19
nssv15647917copy number loss2-1314-002SNP arrayGenotyping14
nssv15648773copy number loss2-1285-003SNP arrayGenotyping26
nssv15649908copy number loss2-1360-002SNP arrayGenotyping23
nssv15650051copy number loss2-1292-003SNP arrayGenotyping17
nssv15652433copy number loss2-1519-002SNP arrayGenotyping18
nssv15652520copy number loss2-1526-003SNP arrayGenotyping14
nssv15653036copy number loss2-1584-003SNP arrayGenotyping20
nssv15653558copy number loss2-1595-001SNP arrayGenotyping24
nssv15654533copy number loss2-1736-003SNP arrayGenotyping20
nssv15654573copy number loss2-1738-003SNP arrayGenotyping22
nssv15655050copy number loss2-1647-003SNP arrayGenotyping26
nssv15655793copy number gain2-1723-003SNP arrayGenotyping29
nssv15657677copy number loss4-0040-002SNP arrayGenotyping15
nssv15658012copy number loss3-0481-000SNP arrayGenotyping17
nssv15661271copy number loss5-0066-002SNP arrayGenotyping14
nssv15661997copy number loss5-0071-003SNP arrayGenotyping21
nssv15664153copy number loss224538SSNP arrayGenotyping24
nssv15665099copy number loss14AG81SNP arrayGenotyping16
nssv15665716copy number loss7-0086-003SNP arrayGenotyping16
nssv15670247copy number gain7-0288-003SNP arrayGenotyping20
nssv15674747copy number loss205648SNP arrayGenotyping18
nssv15681491copy number lossOCD108-1634SNP arrayGenotyping19
nssv15684073copy number lossOCD148-DJ-1487SNP arrayGenotyping18
nssv15684610copy number lossOCD144-SR-1388(189277)SNP arrayGenotyping13
nssv15685665copy number lossOCD169-8961252SNP arrayGenotyping26
nssv15685819copy number lossOCD20-S_896383SNP arrayGenotyping25
nssv15685865copy number lossOCD22-S_896411SNP arrayGenotyping22
nssv15686698copy number gainOCD24-S_896441SNP arrayGenotyping21
nssv15687045copy number lossOCD39-S_0625-1152-2SNP arrayGenotyping27
nssv15687184copy number lossOCD33-S_896593SNP arrayGenotyping25
nssv15687666copy number lossOCD172-SW-1812SNP arrayGenotyping17
nssv15688123copy number loss209355SNP arrayGenotyping28
nssv15688497copy number lossOCD33-S_896591SNP arrayGenotyping29
nssv15689513copy number lossOCD106-1607(313)SNP arrayGenotyping23
nssv15690471copy number lossOCD144-AR-161SNP arrayGenotyping25
nssv15690858copy number lossOCD170-TJ-1809SNP arrayGenotyping25
nssv15691558copy number lossOCD53-S_0625-8346-1SNP arrayGenotyping16
nssv15692175copy number lossOCD65-DS-1248SNP arrayGenotyping14
nssv15692509copy number lossOCD63-JS-1229SNP arrayGenotyping18
nssv15694935copy number loss220177SNP arrayGenotyping25
nssv15695494copy number loss168088SNP arrayGenotyping21
nssv15696265copy number loss157166SNP arrayGenotyping19
nssv15699041copy number loss194735SNP arrayGenotyping21
nssv15699177copy number loss202632SNP arrayGenotyping23
nssv15699235copy number loss213838SNP arrayGenotyping25
nssv15702239copy number loss223142SNP arrayGenotyping18

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15612880RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15613239RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15620788RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15624817RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15624976RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15626952RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15627386RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15627469RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15627583RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15629308RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15629358RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15629733RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15630290RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15631645RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15632056RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15632257RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15632834RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15635644RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15639264RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15640872RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15643540RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15645229RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15645813RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15646263RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15646284RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15646650RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15647224RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15647429RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15647917RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15648773RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15649908RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15650051RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15652433RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15652520RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15653036RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15653558RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15654533RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15654573RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15655050RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15655793RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15657677RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15658012RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15661271RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15661997RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15664153RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15665099RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15665716RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15670247RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15674747RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15681491RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15684073RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15684610RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15685665RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15685819RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15685865RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15686698RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)dup
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15687045RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15687184RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15687666RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15688123RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15688497RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15689513RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15690471RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15690858RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15691558RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15692175RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15692509RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15694935RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15695494RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15696265RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15699041RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15699177RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15699235RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15702239RemappedPerfectNC_000012.12:g.(?_
11067331)_(1110381
4_?)del
GRCh38.p12First PassNC_000012.12Chr1211,067,33111,103,814
nssv15612880Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15613239Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15620788Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15624817Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15624976Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15626952Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15627386Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15627469Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15627583Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15629308Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15629358Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15629733Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15630290Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15631645Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15632056Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15632257Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15632834Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15635644Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15639264Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15640872Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15643540Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)dup
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15645229Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15645813Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15646263Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15646284Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
nssv15646650Submitted genomicNC_000012.11:g.(?_
11219930)_(1125641
3_?)del
GRCh37 (hg19)NC_000012.11Chr1211,219,93011,256,413
Showing 100 of 148

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

Support Center