nsv993379

Organism: Homo sapiens

Study:nstd94 (Helman et al. 2014)
Variant Type:mobile element insertion
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:62
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Helman et al. 2014

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: 465 SVs from 32 studies. See in: genome view

Remapped(Score: Perfect):76,926,746-76,926,746

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv993379	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nsv993379	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000018.9	Chr18	74,638,702	74,638,702

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3318687	mobile element insertion	TCGA-22-1016	Sequencing	Split read and paired-end mapping	218
nssv3318688	mobile element insertion	TCGA-56-1622	Sequencing	Split read and paired-end mapping	883
nssv3318689	mobile element insertion	TCGA-60-2713	Sequencing	Split read and paired-end mapping	989
nssv3318690	mobile element insertion	TCGA-60-2724	Sequencing	Split read and paired-end mapping	883
nssv3318691	mobile element insertion	TCGA-CN-4741	Sequencing	Split read and paired-end mapping	1,041
nssv3318692	mobile element insertion	TCGA-CR-6472	Sequencing	Split read and paired-end mapping	1,043
nssv3318693	mobile element insertion	TCGA-CR-6482	Sequencing	Split read and paired-end mapping	1,338
nssv3318694	mobile element insertion	TCGA-CV-5443	Sequencing	Split read and paired-end mapping	1,331
nssv3318695	mobile element insertion	TCGA-BA-4076	Sequencing	Split read and paired-end mapping	1,051
nssv3318696	mobile element insertion	TCGA-BA-6873	Sequencing	Split read and paired-end mapping	1,110
nssv3318697	mobile element insertion	TCGA-CN-4737	Sequencing	Split read and paired-end mapping	1,125
nssv3318698	mobile element insertion	TCGA-CN-5365	Sequencing	Split read and paired-end mapping	893
nssv3318699	mobile element insertion	TCGA-CN-5374	Sequencing	Split read and paired-end mapping	1,108
nssv3318700	mobile element insertion	TCGA-CR-5250	Sequencing	Split read and paired-end mapping	1,025
nssv3318701	mobile element insertion	TCGA-CR-6467	Sequencing	Split read and paired-end mapping	1,106
nssv3318702	mobile element insertion	TCGA-CV-5442	Sequencing	Split read and paired-end mapping	1,087
nssv3318703	mobile element insertion	TCGA-CV-6433	Sequencing	Split read and paired-end mapping	903
nssv3318704	mobile element insertion	TCGA-CV-7090	Sequencing	Split read and paired-end mapping	927
nssv3318705	mobile element insertion	TCGA-CV-7180	Sequencing	Split read and paired-end mapping	1,136
nssv3318706	mobile element insertion	TCGA-CV-7255	Sequencing	Split read and paired-end mapping	909
nssv3318707	mobile element insertion	TCGA-AP-A052	Sequencing	Split read and paired-end mapping	1,131
nssv3318708	mobile element insertion	TCGA-05-4398	Sequencing	Split read and paired-end mapping	650
nssv3318709	mobile element insertion	TCGA-05-4432	Sequencing	Split read and paired-end mapping	494
nssv3318710	mobile element insertion	TCGA-38-4630	Sequencing	Split read and paired-end mapping	726
nssv3318711	mobile element insertion	TCGA-44-2666	Sequencing	Split read and paired-end mapping	770
nssv3318712	mobile element insertion	TCGA-49-4486	Sequencing	Split read and paired-end mapping	646
nssv3318713	mobile element insertion	TCGA-55-6986	Sequencing	Split read and paired-end mapping	1,151
nssv3318714	mobile element insertion	TCGA-64-1678	Sequencing	Split read and paired-end mapping	733
nssv3318715	mobile element insertion	TCGA-67-3771	Sequencing	Split read and paired-end mapping	869
nssv3318716	mobile element insertion	TCGA-67-6215	Sequencing	Split read and paired-end mapping	613
nssv3318717	mobile element insertion	TCGA-73-4659	Sequencing	Split read and paired-end mapping	739
nssv3318718	mobile element insertion	TCGA-75-5147	Sequencing	Split read and paired-end mapping	1,151
nssv3318719	mobile element insertion	TCGA-02-2485	Sequencing	Split read and paired-end mapping	1,277
nssv3318720	mobile element insertion	TCGA-06-0214	Sequencing	Split read and paired-end mapping	1,101
nssv3318721	mobile element insertion	TCGA-06-0686	Sequencing	Split read and paired-end mapping	1,228
nssv3318722	mobile element insertion	TCGA-06-2557	Sequencing	Split read and paired-end mapping	1,217
nssv3318723	mobile element insertion	TCGA-06-2570	Sequencing	Split read and paired-end mapping	1,113
nssv3318724	mobile element insertion	TCGA-06-5415	Sequencing	Split read and paired-end mapping	1,088
nssv3318725	mobile element insertion	TCGA-14-1823	Sequencing	Split read and paired-end mapping	1,021
nssv3318726	mobile element insertion	TCGA-26-5132	Sequencing	Split read and paired-end mapping	1,130
nssv3318727	mobile element insertion	TCGA-26-5135	Sequencing	Split read and paired-end mapping	1,101
nssv3318728	mobile element insertion	TCGA-27-1831	Sequencing	Split read and paired-end mapping	1,170
nssv3318729	mobile element insertion	TCGA-AB-2978	Sequencing	Split read and paired-end mapping	964
nssv3318730	mobile element insertion	TCGA-A3-3324	Sequencing	Split read and paired-end mapping	871
nssv3318731	mobile element insertion	TCGA-BP-4977	Sequencing	Split read and paired-end mapping	688
nssv3318732	mobile element insertion	TCGA-A3-3370	Sequencing	Split read and paired-end mapping	867
nssv3318733	mobile element insertion	TCGA-A3-3372	Sequencing	Split read and paired-end mapping	973
nssv3318734	mobile element insertion	TCGA-A3-3387	Sequencing	Split read and paired-end mapping	1,198
nssv3318735	mobile element insertion	TCGA-AK-3428	Sequencing	Split read and paired-end mapping	1,164
nssv3318736	mobile element insertion	TCGA-B2-4101	Sequencing	Split read and paired-end mapping	933
nssv3318737	mobile element insertion	TCGA-BP-5168	Sequencing	Split read and paired-end mapping	1,206
nssv3318738	mobile element insertion	TCGA-CJ-4639	Sequencing	Split read and paired-end mapping	1,227
nssv3318739	mobile element insertion	TCGA-CJ-4885	Sequencing	Split read and paired-end mapping	1,191
nssv3318740	mobile element insertion	TCGA-CJ-4899	Sequencing	Split read and paired-end mapping	919
nssv3318741	mobile element insertion	TCGA-CJ-4918	Sequencing	Split read and paired-end mapping	937
nssv3318742	mobile element insertion	TCGA-CJ-5682	Sequencing	Split read and paired-end mapping	1,162
nssv3318743	mobile element insertion	TCGA-CJ-6033	Sequencing	Split read and paired-end mapping	1,342
nssv3318744	mobile element insertion	TCGA-CZ-5987	Sequencing	Split read and paired-end mapping	1,045
nssv3318745	mobile element insertion	TCGA-25-1319	Sequencing	Split read and paired-end mapping	637
nssv3318746	mobile element insertion	TCGA-13-0890	Sequencing	Split read and paired-end mapping	1,187
nssv3318747	mobile element insertion	TCGA-A2-A0D1	Sequencing	Split read and paired-end mapping	1,072
nssv3318748	mobile element insertion	TCGA-AR-A0TX	Sequencing	Split read and paired-end mapping	1,128

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3318687	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318688	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318689	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318690	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318691	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318692	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318693	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318694	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318695	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318696	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318697	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318698	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318699	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318700	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318701	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318702	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318703	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318704	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318705	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318706	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318707	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318708	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318709	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318710	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318711	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318712	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318713	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318714	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318715	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318716	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318717	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318718	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318719	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318720	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318721	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318722	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318723	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318724	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318725	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318726	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318727	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318728	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318729	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318730	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318731	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318732	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318733	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318734	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318735	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318736	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318737	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318738	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318739	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318740	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318741	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318742	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318743	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318744	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318745	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318746	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318747	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318748	Remapped	Perfect	NC_000018.10:g.769 26746_76926747ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	76,926,746	76,926,746
nssv3318687	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318688	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318689	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318690	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318691	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318692	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318693	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318694	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318695	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318696	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318697	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318698	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318699	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318700	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318701	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318702	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318703	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318704	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318705	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318706	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318707	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318708	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318709	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318710	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318711	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318712	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318713	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318714	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318715	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318716	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318717	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318718	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318719	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318720	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318721	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318722	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318723	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702
nssv3318724	Submitted genomic		NC_000018.9:g.7463 8702_74638703ins?	GRCh37 (hg19)		NC_000018.9	Chr18	74,638,702	74,638,702

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dbVar

Database of genomic structural variation

nsv993379

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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