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nsv4387002

  • Variant Calls:71
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:31,783

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 608 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):128,661,752-128,693,534Question Mark
Overlapping variant regions from other studies: 608 SVs from 80 studies. See in: genome view    
Submitted genomic128,380,595-128,412,377Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4387002RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3128,661,752128,693,534
nsv4387002Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3128,380,595128,412,377

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15615726copy number gain1-0777-003SNP arrayGenotyping26
nssv15616783copy number gain1-0802-003SNP arrayGenotyping22
nssv15617296copy number gain1-0838-003SNP arrayGenotyping27
nssv15619652copy number gain1-0955-003SNP arrayGenotyping22
nssv15620122copy number gain1-0940-003SNP arrayGenotyping24
nssv15631603copy number gain10-0001-001SNP arrayGenotyping24
nssv15631948copy number gain1-1061-003SNP arrayGenotyping19
nssv15631970copy number gain1-1062-003SNP arrayGenotyping29
nssv15632373copy number gain10-0004-001SNP arrayGenotyping13
nssv15633122copy number gain10-1118-002SNP arrayGenotyping17
nssv15633939copy number gain10-1155-003SNP arrayGenotyping22
nssv15633960copy number gain10-1155-004SNP arrayGenotyping21
nssv15634180copy number gain10-1155-005SNP arrayGenotyping22
nssv15635141copy number gain13-0029-002SNP arrayGenotyping18
nssv15639036copy number gain14-0246-001SNP arrayGenotyping22
nssv15639057copy number gain14-0246-002SNP arrayGenotyping22
nssv15640678copy number gain14-0376-001SNP arrayGenotyping24
nssv15640718copy number gain14-0376-003SNP arrayGenotyping22
nssv15640729copy number gain14-0376-004SNP arrayGenotyping25
nssv15641018copy number gain14-0323-002SNP arrayGenotyping22
nssv15641226copy number gain14-0295-002SNP arrayGenotyping21
nssv15642232copy number gain16-1002-003SNP arrayGenotyping25
nssv15642553copy number gain15-1132-001SNP arrayGenotyping18
nssv15642669copy number gain14-0356-003SNP arrayGenotyping29
nssv15642696copy number gain14-0356-004SNP arrayGenotyping24
nssv15643304copy number gain14-0364-001SNP arrayGenotyping22
nssv15643856copy number gain16-1005-003SNP arrayGenotyping13
nssv15644107copy number gain2-0126-001SNP arrayGenotyping23
nssv15644301copy number gain16-1005-004SNP arrayGenotyping24
nssv15645698copy number gain16-1021-002SNP arrayGenotyping26
nssv15646472copy number gain2-1189-001SNP arrayGenotyping19
nssv15647250copy number gain2-1086-001SNP arrayGenotyping25
nssv15648343copy number gain2-1287-003SNP arrayGenotyping18
nssv15649341copy number gain2-1375-002SNP arrayGenotyping23
nssv15649378copy number gain2-1379-001SNP arrayGenotyping18
nssv15649449copy number gain2-1401-003SNP arrayGenotyping30
nssv15650160copy number gain2-1303-001SNP arrayGenotyping16
nssv15650373copy number gain2-1341-003SNP arrayGenotyping25
nssv15651943copy number gain2-1497-003SNP arrayGenotyping21
nssv15653236copy number gain2-1638-003SNP arrayGenotyping22
nssv15654653copy number gain3-0178-000SNP arrayGenotyping25
nssv15655765copy number gain2-1721-003SNP arrayGenotyping29
nssv15655785copy number gain2-1722-003SNP arrayGenotyping15
nssv15656919copy number gain3-0664-000SNP arrayGenotyping26
nssv15660825copy number gain4-0034-004SNP arrayGenotyping21
nssv15661013copy number gain4-0069-004SNP arrayGenotyping21
nssv15661964copy number gain5-0071-001SNP arrayGenotyping26
nssv15664808copy number gain5-0025-001SNP arrayGenotyping22
nssv15667407copy number gain7-0184-003SNP arrayGenotyping22
nssv15667625copy number gain5-1000-001SNP arrayGenotyping21
nssv15668422copy number gain7-0204-003SNP arrayGenotyping22
nssv15668767copy number gain7-0226-003SNP arrayGenotyping14
nssv15669351copy number gain7-0221-003SNP arrayGenotyping16
nssv15671301copy number gain7-0280-004SNP arrayGenotyping17
nssv15671343copy number gain7-0280-007SNP arrayGenotyping21
nssv15672304copy number gain7-0311-003SNP arrayGenotyping24
nssv15675881copy number gain211610SNP arrayGenotyping17
nssv15680505copy number gain213165SNP arrayGenotyping24
nssv15680624copy number gain214104SNP arrayGenotyping18
nssv15682859copy number gainOCD1157-HAM493SNP arrayGenotyping25
nssv15683804copy number gainOCD13-S_896242SNP arrayGenotyping29
nssv15683883copy number gainOCD136-896482SNP arrayGenotyping16
nssv15686167copy number gainOCD2-B_MA-1288SNP arrayGenotyping21
nssv15686207copy number gainOCD20-S_896382SNP arrayGenotyping23
nssv15689211copy number gain234384SNP arrayGenotyping23
nssv15689666copy number gainOCD1120-896013SNP arrayGenotyping22
nssv15691679copy number gainOCD75-JB-1215SNP arrayGenotyping23
nssv15692145copy number gainOCD64-EF-1420SNP arrayGenotyping18
nssv15692535copy number gainOCD65-RS-1249SNP arrayGenotyping21
nssv15700246copy number gain196898SNP arrayGenotyping16
nssv15702007copy number gain200018SNP arrayGenotyping18

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15615726RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15616783RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15617296RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15619652RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15620122RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15631603RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15631948RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15631970RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15632373RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15633122RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15633939RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15633960RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15634180RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15635141RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15639036RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15639057RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15640678RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15640718RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15640729RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15641018RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15641226RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15642232RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15642553RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15642669RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15642696RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15643304RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15643856RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15644107RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15644301RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15645698RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15646472RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15647250RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15648343RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15649341RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15649378RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15649449RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15650160RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15650373RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15651943RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15653236RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15654653RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15655765RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15655785RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15656919RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15660825RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15661013RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15661964RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15664808RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15667407RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15667625RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15668422RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15668767RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15669351RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15671301RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15671343RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15672304RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15675881RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15680505RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15680624RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15682859RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15683804RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15683883RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15686167RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15686207RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15689211RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15689666RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15691679RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15692145RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15692535RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15700246RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15702007RemappedPerfectNC_000003.12:g.(?_
128661752)_(128693
534_?)dup
GRCh38.p12First PassNC_000003.12Chr3128,661,752128,693,534
nssv15615726Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15616783Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15617296Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15619652Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15620122Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15631603Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15631948Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15631970Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15632373Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15633122Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15633939Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15633960Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15634180Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15635141Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15639036Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15639057Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15640678Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15640718Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15640729Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15641018Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15641226Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15642232Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15642553Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15642669Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15642696Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15643304Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15643856Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15644107Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
nssv15644301Submitted genomicNC_000003.11:g.(?_
128380595)_(128412
377_?)dup
GRCh37 (hg19)NC_000003.11Chr3128,380,595128,412,377
Showing 100 of 142

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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