msrb1[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
nsv3898566	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 1,991,251-1,997,211 , GRCh38.p12 chr16: 1,941,250-1,947,210	MSRB1, RPL3L
nsv4455594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-2,053,328 , GRCh38.p12 chr16: 35,880-2,003,327	MSRB1, JPT2, 128 more genes
nsv3919589	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 36,766-1,987,584 , GRCh37 chr16: 96,766-2,047,583 , GRCh38 chr16: 46,766-1,997,582	MSRB1, C1QTNF8, 127 more genes
nsv4683390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004	MSRB1, 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	MSRB1, 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	MSRB1, 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	MSRB1, 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	MSRB1, 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	MSRB1, NHERF2, 37 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	MSRB1, 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	MSRB1, NPW, 21 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	MSRB1, 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	MSRB1, 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	MSRB1, 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	MSRB1, 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	MSRB1, 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	MSRB1, BMERB1, 701 more genes
nsv3903116	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-22,442,007 , GRCh38.p12 chr16: 35,880-22,430,686	MSRB1, NPIPA8, 616 more genes
nsv3900978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-19,806,921 , GRCh38.p12 chr16: 35,880-19,795,599	MSRB1, LOC105371091, 543 more genes
nsv3915829	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 656,663-15,744,462 , GRCh38 chr16: 666,662-15,743,104 , GRCh37 chr16: 716,662-15,836,961	MSRB1, RPL35AP34, 429 more genes

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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

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Items: 1 to 20 of 54

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Number of Variants: 20

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