npw[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4683390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004	NPW, MRPS34, 102 more genes
nsv4449893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,115,656 , GRCh38.p12 chr16: 574,055-2,065,655	NPW, LMF1-AS1, 99 more genes
nsv7098880	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378	NPW, TPSP1, 78 more genes
nsv4683209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,203,718-2,185,710 , GRCh38.p12 chr16: 1,153,718-2,135,709	NPW, TMEM204, 67 more genes
nsv3893007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,734,363-2,285,561 , GRCh38.p12 chr16: 1,684,362-2,235,560	NPW, IGFALS, 49 more genes
nsv4682253	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,573,499-2,114,448 , GRCh38.p12 chr16: 1,523,498-2,064,447	NPW, NHERF2, 37 more genes
nsv6637664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,021,144-2,266,791 , GRCh38.p12 chr16: 1,971,143-2,216,790	NPW, SNHG19, 22 more genes
nsv6289860	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 1,851,807-2,093,151 , GRCh37.p13 chr16: 1,901,808-2,143,152	NPW, HS3ST6, 24 more genes
nsv6315059	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 1,903,155-2,093,402 , GRCh37.p13 chr16: 1,953,156-2,143,403	NPW, HS3ST6, 21 more genes
nsv6637964	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,021,144-2,146,432 , GRCh38.p12 chr16: 1,971,143-2,096,431	NPW, NTHL1, 11 more genes
nsv6309997	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,003,468-2,126,543 , GRCh38.p12 chr16: 1,953,467-2,076,542	NPW, NHERF2, 16 more genes
nsv7094763	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,034,220-2,152,787 , GRCh38.p12 chr16: 1,984,219-2,102,786	NPW, NHERF2, 10 more genes
nsv6309998	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,034,220-2,136,892 , GRCh38.p12 chr16: 1,984,219-2,086,891	NPW, SYNGR3, 8 more genes
nsv6310065	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,029,297-2,096,295 , GRCh38.p12 chr16: 1,979,296-2,046,294	NPW, TSC2, 8 more genes
nsv3906108	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224	NPW, CKLF, 1882 more genes
nsv3904593	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973	NPW, LOC100128079, 1879 more genes
nsv3901410	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287	NPW, LINC02175, 1877 more genes
nsv3909417	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-90,163,275 , GRCh38.p12 chr16: 38,165-90,096,867	NPW, PRSS53, 1868 more genes
nsv3892266	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-90,155,062 , GRCh38.p12 chr16: 35,881-90,088,654	NPW, FTLP14, 1868 more genes
nsv1398297	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 102,839-28,327,676 , GRCh38.p12 chr16: 52,839-28,316,355	NPW, BMERB1, 701 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 66

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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