dbVar data for all organisms

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Variant Placements for nstd152 (displaying 100 of 103985 variants)
Study ID	Variant ID	Variant Region type	Validation	Assembly	Accession	Chr	Outer-Start	Start	Inner-Start	Inner-End	End	Outer-End	Placement Type
nstd152	nsv3172122	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		191407			193038		Submitted genomic
nstd152	nsv3172122	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		191407			193038		Submitted genomic
nstd152	nsv3172171	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		90407			90466		Submitted genomic
nstd152	nsv3172171	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		90407			90466		Submitted genomic
nstd152	nsv3175064	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		714325			714375		Submitted genomic
nstd152	nsv3175064	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		714325			714375		Submitted genomic
nstd152	nsv3176824	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		831217			833736		Submitted genomic
nstd152	nsv3176824	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		831217			833736		Submitted genomic
nstd152	nsv3176959	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		669514			669588		Submitted genomic
nstd152	nsv3176959	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		669514			669588		Submitted genomic
nstd152	nsv3177862	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		140141			143548		Submitted genomic
nstd152	nsv3177862	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		140141			143548		Submitted genomic
nstd152	nsv3178769	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		814625			814721		Submitted genomic
nstd152	nsv3178769	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		814625			814721		Submitted genomic
nstd152	nsv3179418	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		137221			137339		Submitted genomic
nstd152	nsv3179418	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		137221			137339		Submitted genomic
nstd152	nsv3179493	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		853564			853713		Submitted genomic
nstd152	nsv3179493	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		853564			853713		Submitted genomic
nstd152	nsv3180409	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		610348			610416		Submitted genomic
nstd152	nsv3180409	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		610348			610416		Submitted genomic
nstd152	nsv3181490	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		610044			610108		Submitted genomic
nstd152	nsv3181490	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		610044			610108		Submitted genomic
nstd152	nsv3181790	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		737102			740486		Submitted genomic
nstd152	nsv3181790	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		737102			740486		Submitted genomic
nstd152	nsv3184312	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		732377			735779		Submitted genomic
nstd152	nsv3184312	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		732377			735779		Submitted genomic
nstd152	nsv3184590	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		180321			180372		Submitted genomic
nstd152	nsv3184590	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		180321			180372		Submitted genomic
nstd152	nsv3184768	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		609341			609409		Submitted genomic
nstd152	nsv3184768	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		609341			609409		Submitted genomic
nstd152	nsv3184815	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		820920			820970		Submitted genomic
nstd152	nsv3184815	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		820920			820970		Submitted genomic
nstd152	nsv3189315	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		136212			136309		Submitted genomic
nstd152	nsv3189315	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		136212			136309		Submitted genomic
nstd152	nsv3190022	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		90136			90195		Submitted genomic
nstd152	nsv3190022	complex substitution	No	GRCh38 (hg38)	NC_000001.11	1		90136			90195		Submitted genomic
nstd152	nsv3192546	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		904047			905646		Submitted genomic
nstd152	nsv3192546	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		904047			905646		Submitted genomic
nstd152	nsv3192608	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	38481	41001	43521	77309	79829	82349	Submitted genomic
nstd152	nsv3192608	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	38481	41001	43521	77309	79829	82349	Submitted genomic
nstd152	nsv3197740	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	909064	909393	909722	913967	914296	914625	Submitted genomic
nstd152	nsv3197740	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	909064	909393	909722	913967	914296	914625	Submitted genomic
nstd152	nsv3199266	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	903718	904047	904376	905317	905646	905975	Submitted genomic
nstd152	nsv3199266	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	903718	904047	904376	905317	905646	905975	Submitted genomic
nstd152	nsv3199295	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	608157					615217	Submitted genomic
nstd152	nsv3199295	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	608157					615217	Submitted genomic
nstd152	nsv3200228	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	722571					742452	Submitted genomic
nstd152	nsv3200228	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	722571					742452	Submitted genomic
nstd152	nsv3201037	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	820561	820573	820585	820876	820888	820900	Submitted genomic
nstd152	nsv3201037	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	820561	820573	820585	820876	820888	820900	Submitted genomic
nstd152	nsv3202214	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	766904	767233	767562	788410	788739	789068	Submitted genomic
nstd152	nsv3202214	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	766904	767233	767562	788410	788739	789068	Submitted genomic
nstd152	nsv3203191	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	853400	853415	853430	853792	853807	853822	Submitted genomic
nstd152	nsv3203191	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	853400	853415	853430	853792	853807	853822	Submitted genomic
nstd152	nsv3204181	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	826970					835462	Submitted genomic
nstd152	nsv3204181	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	826970					835462	Submitted genomic
nstd152	nsv3206703	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		608157			615217		Submitted genomic
nstd152	nsv3206703	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		608157			615217		Submitted genomic
nstd152	nsv3206957	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	821822	822151	822480	826025	826354	826683	Submitted genomic
nstd152	nsv3206957	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	821822	822151	822480	826025	826354	826683	Submitted genomic
nstd152	nsv3208987	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	930684					940927	Submitted genomic
nstd152	nsv3208987	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1	930684					940927	Submitted genomic
nstd152	nsv3212875	insertion	No	GRCh38 (hg38)	NC_000001.11	1	779146					796325	Submitted genomic
nstd152	nsv3212875	insertion	No	GRCh38 (hg38)	NC_000001.11	1	779146					796325	Submitted genomic
nstd152	nsv3215117	insertion	No	GRCh38 (hg38)	NC_000001.11	1	137901					142869	Submitted genomic
nstd152	nsv3215117	insertion	No	GRCh38 (hg38)	NC_000001.11	1	137901					142869	Submitted genomic
nstd152	nsv3215982	insertion	No	GRCh38 (hg38)	NC_000001.11	1	132349					142869	Submitted genomic
nstd152	nsv3215982	insertion	No	GRCh38 (hg38)	NC_000001.11	1	132349					142869	Submitted genomic
nstd152	nsv3217324	insertion	No	GRCh38 (hg38)	NC_000001.11	1	847392					889224	Submitted genomic
nstd152	nsv3217324	insertion	No	GRCh38 (hg38)	NC_000001.11	1	847392					889224	Submitted genomic
nstd152	nsv3218940	insertion	No	GRCh38 (hg38)	NC_000001.11	1	865008					940927	Submitted genomic
nstd152	nsv3218940	insertion	No	GRCh38 (hg38)	NC_000001.11	1	865008					940927	Submitted genomic
nstd152	nsv3223226	insertion	No	GRCh38 (hg38)	NC_000001.11	1	653276					693482	Submitted genomic
nstd152	nsv3223226	insertion	No	GRCh38 (hg38)	NC_000001.11	1	653276					693482	Submitted genomic
nstd152	nsv3227952	insertion	No	GRCh38 (hg38)	NC_000001.11	1	728601					742452	Submitted genomic
nstd152	nsv3227952	insertion	No	GRCh38 (hg38)	NC_000001.11	1	728601					742452	Submitted genomic
nstd152	nsv3228037	insertion	No	GRCh38 (hg38)	NC_000001.11	1	865008					889402	Submitted genomic
nstd152	nsv3228037	insertion	No	GRCh38 (hg38)	NC_000001.11	1	865008					889402	Submitted genomic
nstd152	nsv3228226	insertion	No	GRCh38 (hg38)	NC_000001.11	1	379971					396993	Submitted genomic
nstd152	nsv3228226	insertion	No	GRCh38 (hg38)	NC_000001.11	1	379971					396993	Submitted genomic
nstd152	nsv3228508	insertion	No	GRCh38 (hg38)	NC_000001.11	1	865008					889224	Submitted genomic
nstd152	nsv3228508	insertion	No	GRCh38 (hg38)	NC_000001.11	1	865008					889224	Submitted genomic
nstd152	nsv3247706	sequence alteration	No	GRCh38 (hg38)	NC_000001.11	1	831052	831055	831058	833722	833732	833744	Submitted genomic
nstd152	nsv3247706	sequence alteration	No	GRCh38 (hg38)	NC_000001.11	1	831052	831055	831058	833722	833732	833744	Submitted genomic
nstd152	nsv3279658	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		934807			934919		Submitted genomic
nstd152	nsv3279658	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		934807			934919		Submitted genomic
nstd152	nsv3279779	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		934218			934750		Submitted genomic
nstd152	nsv3279779	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		934218			934750		Submitted genomic
nstd152	nsv3279831	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		609436			609636		Submitted genomic
nstd152	nsv3279831	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		609436			609636		Submitted genomic
nstd152	nsv3279853	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		181325			181448		Submitted genomic
nstd152	nsv3279853	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		181325			181448		Submitted genomic
nstd152	nsv3279887	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		853590			853642		Submitted genomic
nstd152	nsv3279887	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		853590			853642		Submitted genomic
nstd152	nsv3280519	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		909396			909487		Submitted genomic
nstd152	nsv3280519	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		909396			909487		Submitted genomic
nstd152	nsv3280640	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		933966			934498		Submitted genomic
nstd152	nsv3280640	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		933966			934498		Submitted genomic
nstd152	nsv3280707	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		872544			872754		Submitted genomic
nstd152	nsv3280707	copy number variation	No	GRCh38 (hg38)	NC_000001.11	1		872544			872754		Submitted genomic

dbVar

Database of genomic structural variation

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