dbVar data for all organisms

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Variant Placements for nstd206 (displaying 100 of 173332 variants)
Study ID	Variant ID	Variant Region type	Validation	Assembly	Accession	Chr	Outer-Start	Start	Inner-Start	Inner-End	End	Outer-End	Placement Type
nstd206	nsv5397415	mobile element insertion	No	GRCh38 (hg38)	NC_000001.11	1		852829			852880		Submitted genomic
nstd206	nsv5397415	mobile element insertion	No	GRCh38 (hg38)	NC_000001.11	1		852829			852880		Submitted genomic
nstd206	nsv5401906	mobile element insertion	No	GRCh38 (hg38)	NC_000001.11	1		866135			866186		Submitted genomic
nstd206	nsv5401906	mobile element insertion	No	GRCh38 (hg38)	NC_000001.11	1		866135			866186		Submitted genomic
nstd206	nsv5411887	mobile element insertion	No	GRCh38 (hg38)	NC_000001.11	1		758508			758559		Submitted genomic
nstd206	nsv5411887	mobile element insertion	No	GRCh38 (hg38)	NC_000001.11	1		758508			758559		Submitted genomic
nstd206	nsv5414372	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		938039			938669		Submitted genomic
nstd206	nsv5414372	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		938039			938669		Submitted genomic
nstd206	nsv5414505	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1134549			1134673		Submitted genomic
nstd206	nsv5414505	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1134549			1134673		Submitted genomic
nstd206	nsv5414608	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1227243	1227325	1227389	1227359	1227457	1227477	Submitted genomic
nstd206	nsv5414608	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1227243	1227325	1227389	1227359	1227457	1227477	Submitted genomic
nstd206	nsv5415252	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		895253			899112		Submitted genomic
nstd206	nsv5415252	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		895253			899112		Submitted genomic
nstd206	nsv5415470	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		884607			891019		Submitted genomic
nstd206	nsv5415470	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		884607			891019		Submitted genomic
nstd206	nsv5415870	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		859112			864158		Submitted genomic
nstd206	nsv5415870	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		859112			864158		Submitted genomic
nstd206	nsv5416609	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1201813			1202690		Submitted genomic
nstd206	nsv5416609	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1201813			1202690		Submitted genomic
nstd206	nsv5417411	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		948661			948730		Submitted genomic
nstd206	nsv5417411	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		948661			948730		Submitted genomic
nstd206	nsv5418742	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1164215			1164761		Submitted genomic
nstd206	nsv5418742	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1164215			1164761		Submitted genomic
nstd206	nsv5418973	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1133932			1138406		Submitted genomic
nstd206	nsv5418973	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1133932			1138406		Submitted genomic
nstd206	nsv5419146	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		28000			140000		Submitted genomic
nstd206	nsv5419146	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		28000			140000		Submitted genomic
nstd206	nsv5419302	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		831216			833732		Submitted genomic
nstd206	nsv5419302	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		831216			833732		Submitted genomic
nstd206	nsv5419959	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1134839			1135354		Submitted genomic
nstd206	nsv5419959	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1134839			1135354		Submitted genomic
nstd206	nsv5420430	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1084542			1084626		Submitted genomic
nstd206	nsv5420430	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1084542			1084626		Submitted genomic
nstd206	nsv5420615	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		731375			739994		Submitted genomic
nstd206	nsv5420615	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		731375			739994		Submitted genomic
nstd206	nsv5420952	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1134571			1135362		Submitted genomic
nstd206	nsv5420952	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1134571			1135362		Submitted genomic
nstd206	nsv5421003	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		811384			811817		Submitted genomic
nstd206	nsv5421003	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		811384			811817		Submitted genomic
nstd206	nsv5421515	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		585988			596000		Submitted genomic
nstd206	nsv5421515	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		585988			596000		Submitted genomic
nstd206	nsv5421839	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	793973	793983	793992	893045	893055	893064	Submitted genomic
nstd206	nsv5421839	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	793973	793983	793992	893045	893055	893064	Submitted genomic
nstd206	nsv5422147	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		182000			206000		Submitted genomic
nstd206	nsv5422147	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		182000			206000		Submitted genomic
nstd206	nsv5422255	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		761567			762117		Submitted genomic
nstd206	nsv5422255	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		761567			762117		Submitted genomic
nstd206	nsv5422314	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1207339			1207760		Submitted genomic
nstd206	nsv5422314	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1207339			1207760		Submitted genomic
nstd206	nsv5422961	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		731650			915000		Submitted genomic
nstd206	nsv5422961	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		731650			915000		Submitted genomic
nstd206	nsv5423309	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		917445			917517		Submitted genomic
nstd206	nsv5423309	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		917445			917517		Submitted genomic
nstd206	nsv5423417	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		778728			778780		Submitted genomic
nstd206	nsv5423417	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		778728			778780		Submitted genomic
nstd206	nsv5423684	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		261666			287666		Submitted genomic
nstd206	nsv5423684	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		261666			287666		Submitted genomic
nstd206	nsv5423787	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		822676			822759		Submitted genomic
nstd206	nsv5423787	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		822676			822759		Submitted genomic
nstd206	nsv5423978	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1060224			1060357		Submitted genomic
nstd206	nsv5423978	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1060224			1060357		Submitted genomic
nstd206	nsv5424358	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1248061			1248317		Submitted genomic
nstd206	nsv5424358	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1248061			1248317		Submitted genomic
nstd206	nsv5425170	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1134739			1134842		Submitted genomic
nstd206	nsv5425170	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1134739			1134842		Submitted genomic
nstd206	nsv5426044	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1098995	1099016	1099025	1099889	1099903	1099955	Submitted genomic
nstd206	nsv5426044	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1098995	1099016	1099025	1099889	1099903	1099955	Submitted genomic
nstd206	nsv5426187	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1108212	1108232	1108252	1108672	1108692	1108712	Submitted genomic
nstd206	nsv5426187	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1108212	1108232	1108252	1108672	1108692	1108712	Submitted genomic
nstd206	nsv5426763	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	819743	820254	821016	822123	822868	823549	Submitted genomic
nstd206	nsv5426763	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	819743	820254	821016	822123	822868	823549	Submitted genomic
nstd206	nsv5428547	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1149937			1154604		Submitted genomic
nstd206	nsv5428547	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1149937			1154604		Submitted genomic
nstd206	nsv5428923	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1011741			1012621		Submitted genomic
nstd206	nsv5428923	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1011741			1012621		Submitted genomic
nstd206	nsv5429781	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1240648			1240700		Submitted genomic
nstd206	nsv5429781	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1240648			1240700		Submitted genomic
nstd206	nsv5430171	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		628900			635988		Submitted genomic
nstd206	nsv5430171	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		628900			635988		Submitted genomic
nstd206	nsv5430302	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1141434			1141537		Submitted genomic
nstd206	nsv5430302	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1141434			1141537		Submitted genomic
nstd206	nsv5431065	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1141147			1143332		Submitted genomic
nstd206	nsv5431065	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1141147			1143332		Submitted genomic
nstd206	nsv5431351	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1225673			1226358		Submitted genomic
nstd206	nsv5431351	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1225673			1226358		Submitted genomic
nstd206	nsv5431403	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		751988			775988		Submitted genomic
nstd206	nsv5431403	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		751988			775988		Submitted genomic
nstd206	nsv5431467	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1084112			1084439		Submitted genomic
nstd206	nsv5431467	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1084112			1084439		Submitted genomic
nstd206	nsv5431652	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1123513	1123533	1123553	1123578	1123583	1123603	Submitted genomic
nstd206	nsv5431652	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1123513	1123533	1123553	1123578	1123583	1123603	Submitted genomic
nstd206	nsv5431903	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		962421			963103		Submitted genomic
nstd206	nsv5431903	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		962421			963103		Submitted genomic
nstd206	nsv5432017	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		803230			806636		Submitted genomic
nstd206	nsv5432017	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		803230			806636		Submitted genomic
nstd206	nsv5432085	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1068732			1068834		Submitted genomic
nstd206	nsv5432085	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		1068732			1068834		Submitted genomic
nstd206	nsv5432093	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1029550	1029628	1029721	1029856	1029968	1030038	Submitted genomic
nstd206	nsv5432093	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	1029550	1029628	1029721	1029856	1029968	1030038	Submitted genomic

dbVar

Database of genomic structural variation

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