nsv4378764

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:65
Validation:Not tested
Clinical Assertions: No
Region Size:23,850

Publication(s):Zarrei et al. 2019

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 407 SVs from 66 studies. See in: genome view

Remapped(Score: Perfect):122,598,665-122,622,514

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4378764	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nsv4378764	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	124,358,181	124,382,030

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15611615	copy number loss	1-0650-003	SNP array	Genotyping	18
nssv15612000	copy number loss	1-0640-003	SNP array	Genotyping	19
nssv15613581	copy number loss	1-0691-003	SNP array	Genotyping	26
nssv15614139	copy number gain	1-0746-003	SNP array	Genotyping	21
nssv15615327	copy number loss	1-0769-003	SNP array	Genotyping	24
nssv15616917	copy number loss	1-0826-003	SNP array	Genotyping	27
nssv15616952	copy number loss	1-0826-004	SNP array	Genotyping	17
nssv15618376	copy number loss	1-0868-003	SNP array	Genotyping	29
nssv15619438	copy number loss	1-0922-003	SNP array	Genotyping	16
nssv15619672	copy number loss	1-0957-003	SNP array	Genotyping	20
nssv15620108	copy number loss	1-0940-003	SNP array	Genotyping	24
nssv15621127	copy number loss	1-1010-002	SNP array	Genotyping	26
nssv15621356	copy number loss	1-1015-001	SNP array	Genotyping	21
nssv15622321	copy number loss	1-1028-003	SNP array	Genotyping	22
nssv15622621	copy number loss	1-0255-002	SNP array	Genotyping	15
nssv15623458	copy number loss	1-0261-002	SNP array	Genotyping	21
nssv15623720	copy number loss	1-0275-003	SNP array	Genotyping	27
nssv15626407	copy number loss	1-0051-006	SNP array	Genotyping	32
nssv15629340	copy number loss	1-0541-004	SNP array	Genotyping	15
nssv15629838	copy number loss	1-0580-003	SNP array	Genotyping	33
nssv15632112	copy number loss	10-0011-002	SNP array	Genotyping	28
nssv15633164	copy number loss	11-0011-003	SNP array	Genotyping	19
nssv15634452	copy number loss	11-0041-004	SNP array	Genotyping	16
nssv15635658	copy number loss	11-0051-004	SNP array	Genotyping	30
nssv15639199	copy number loss	14-0277-002	SNP array	Genotyping	19
nssv15639262	copy number loss	14-0284-003	SNP array	Genotyping	25
nssv15640072	copy number loss	14-0103-002	SNP array	Genotyping	23
nssv15641545	copy number loss	14-0154-002	SNP array	Genotyping	15
nssv15642608	copy number loss	15-1133-002	SNP array	Genotyping	14
nssv15643188	copy number loss	14-0358-002	SNP array	Genotyping	30
nssv15643510	copy number loss	16-1013-002	SNP array	Genotyping	27
nssv15644131	copy number loss	15-1131-004	SNP array	Genotyping	20
nssv15644312	copy number loss	16-1006-001	SNP array	Genotyping	24
nssv15644592	copy number loss	15-1134-002	SNP array	Genotyping	25
nssv15647343	copy number loss	2-1238-003	SNP array	Genotyping	19
nssv15649869	copy number loss	2-1359-002	SNP array	Genotyping	14
nssv15651717	copy number loss	2-1547-003	SNP array	Genotyping	13
nssv15653042	copy number loss	2-1620-003	SNP array	Genotyping	26
nssv15653173	copy number loss	2-1626-003	SNP array	Genotyping	23
nssv15658219	copy number loss	4-0001-002	SNP array	Genotyping	14
nssv15660682	copy number loss	5-0039-003	SNP array	Genotyping	19
nssv15663224	copy number loss	4-0061-001	SNP array	Genotyping	32
nssv15664978	copy number loss	14AG933	SNP array	Genotyping	17
nssv15665448	copy number loss	7-0061-003	SNP array	Genotyping	32
nssv15666963	copy number loss	7-0145-003	SNP array	Genotyping	30
nssv15668114	copy number loss	7-0197-003	SNP array	Genotyping	22
nssv15668445	copy number loss	7-0222-003	SNP array	Genotyping	25
nssv15668636	copy number loss	7-0212-003	SNP array	Genotyping	19
nssv15668706	copy number loss	7-0215-003	SNP array	Genotyping	23
nssv15671683	copy number loss	9-0004-001	SNP array	Genotyping	25
nssv15674080	copy number loss	9-0040-002	SNP array	Genotyping	20
nssv15675309	copy number loss	230096S	SNP array	Genotyping	17
nssv15676623	copy number loss	176714	SNP array	Genotyping	18
nssv15676705	copy number loss	189062	SNP array	Genotyping	17
nssv15676796	copy number loss	174265	SNP array	Genotyping	18
nssv15679226	copy number loss	227875	SNP array	Genotyping	22
nssv15681664	copy number loss	214416S	SNP array	Genotyping	21
nssv15682122	copy number loss	219365	SNP array	Genotyping	22
nssv15682846	copy number loss	OCD1157-HAM493	SNP array	Genotyping	25
nssv15683179	copy number loss	OCD1000-S_896253	SNP array	Genotyping	27
nssv15684203	copy number loss	OCD112-B_1664	SNP array	Genotyping	19
nssv15684760	copy number loss	OCD155-AT-1238(190120)	SNP array	Genotyping	15
nssv15692062	copy number loss	OCD61-BC-1271--51	SNP array	Genotyping	20
nssv15701089	copy number loss	205687	SNP array	Genotyping	23
nssv15702087	copy number loss	210574	SNP array	Genotyping	23

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15611615	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15612000	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15613581	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15614139	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)dup	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15615327	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15616917	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15616952	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15618376	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15619438	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15619672	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15620108	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15621127	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15621356	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15622321	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15622621	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15623458	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15623720	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15626407	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15629340	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15629838	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15632112	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15633164	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15634452	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15635658	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15639199	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15639262	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15640072	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15641545	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15642608	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15643188	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15643510	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15644131	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15644312	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15644592	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15647343	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15649869	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15651717	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15653042	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15653173	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15658219	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15660682	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15663224	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15664978	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15665448	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15666963	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15668114	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15668445	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15668636	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15668706	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15671683	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15674080	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15675309	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15676623	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15676705	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15676796	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15679226	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15681664	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15682122	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15682846	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15683179	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15684203	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15684760	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15692062	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15701089	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15702087	Remapped	Perfect	NC_000010.11:g.(?_ 122598665)_(122622 514_?)del	GRCh38.p12	First Pass	NC_000010.11	Chr10	122,598,665	122,622,514
nssv15611615	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15612000	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15613581	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15614139	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)dup	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15615327	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15616917	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15616952	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15618376	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15619438	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15619672	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15620108	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15621127	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15621356	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15622321	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15622621	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15623458	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15623720	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15626407	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15629340	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15629838	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15632112	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15633164	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15634452	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15635658	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15639199	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15639262	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15640072	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15641545	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15642608	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15643188	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15643510	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15644131	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15644312	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15644592	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030
nssv15647343	Submitted genomic		NC_000010.10:g.(?_ 124358181)_(124382 030_?)del	GRCh37 (hg19)		NC_000010.10	Chr10	124,358,181	124,382,030

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dbVar

Database of genomic structural variation

nsv4378764

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

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