rsbn1l[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
nsv3894469	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 77,303,478-77,529,426 , GRCh38.p12 chr7: 77,674,161-77,900,109	RSBN1L, APTR, 3 more genes
nsv3893671	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 77,366,523-77,451,161 , GRCh38.p12 chr7: 77,737,206-77,821,844	RSBN1L, TMEM60, 1 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	RSBN1L, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	RSBN1L, LOC107986817, 2014 more genes
nsv3918722	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 71,225,344-81,735,657 , GRCh37 chr7: 70,690,330-81,364,973 , NCBI36 chr7: 70,328,266-81,202,909	RSBN1L, GTF2IP1, 184 more genes
nsv3922762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 73,992,744-83,618,176 , GRCh38 chr7: 73,873,420-83,988,860 , NCBI36 chr7: 72,925,686-83,456,112	RSBN1L, PMS2P3, 142 more genes
nsv3911276	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 69,382,353-77,823,832 , GRCh37 chr7: 68,847,339-77,453,149 , NCBI36 chr7: 68,485,275-77,291,085	RSBN1L, POM121, 155 more genes
nsv3917211	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 74,377,395-82,031,742 , NCBI36 chr7: 73,429,661-81,498,994 , GRCh37 chr7: 73,992,744-81,661,058	RSBN1L, HSPB1, 123 more genes
nsv6313880	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 77,310,644-84,461,089 , GRCh38.p12 chr7: 77,681,327-84,831,773	RSBN1L, RNU6-337P, 54 more genes
nsv3902523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 75,588,704-80,277,632 , GRCh38.p12 chr7: 75,959,386-80,648,316	RSBN1L, GSAP, 72 more genes
nsv6290688	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 75,058,300-79,083,658 , GRCh37.p13 chr7: 75,921,853-78,712,974	RSBN1L, GTF2IP1, 76 more genes
nsv3921264	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 74,963,960-77,842,828 , GRCh37 chr7: 75,126,024-78,004,892 , GRCh38 chr7: 75,496,701-78,375,575	RSBN1L, PMS2P11, 56 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	RSBN1L, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	RSBN1L, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	RSBN1L, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	RSBN1L, TRGV3, 2682 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	RSBN1L, AOC1, 2682 more genes
nsv4352523	inversion	1	nstd102	human	Pathogenic	GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550	RSBN1L, ACHE, 1532 more genes
nsv3919663	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr7: 71,282,013-78,631,323 , GRCh37 chr7: 71,644,077-78,793,387 , GRCh38 chr7: 72,179,092-79,164,071	RSBN1L, CLDN4, 149 more genes
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	RSBN1L, RRBP1P1, 2680 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 24

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Number of Variants: 20

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