crygn[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
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	CRYGN, RNU6-438P, 2682 more genes
nsv4675615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620	CRYGN, ATG9B, 603 more genes
nsv3915633	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 134,002,121-158,077,335 , GRCh38 chr7: 134,666,829-158,591,882 , GRCh37 chr7: 134,351,581-158,384,574	CRYGN, MOXD2P, 561 more genes
nsv3897512	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 137,917,376-159,119,707 , GRCh38.p12 chr7: 138,232,630-159,327,017	CRYGN, LOC105375548, 520 more genes
nsv3903590	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,133,025-158,982,771 , GRCh38.p12 chr7: 140,433,225-159,190,080	CRYGN, LOC105375597, 468 more genes
nsv3910344	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 140,754,198-159,307,523 , GRCh37 chr7: 140,453,998-159,100,212 , NCBI36 chr7: 140,100,467-158,792,973	CRYGN, LOC112268012, 461 more genes
nsv3905379	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 140,636,858-159,119,707 , GRCh38.p12 chr7: 140,937,058-159,327,017	CRYGN, AGAP3, 459 more genes
nsv3919772	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 141,307,130-158,821,317 , GRCh37 chr7: 142,528,609-159,128,556 , GRCh38 chr7: 141,960,861-159,335,866	CRYGN, LOC105375567, 429 more genes
nsv3904188	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 141,938,235-159,126,310 , GRCh38.p12 chr7: 142,288,582-159,333,620	CRYGN, RBM33-DT, 423 more genes
nsv3915683	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 143,884,559-159,282,390 , GRCh37 chr7: 143,581,652-159,075,079 , NCBI36 chr7: 143,212,585-158,767,840	CRYGN, FASTK, 280 more genes
nsv3907788	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 143,839,360-159,138,663 , GRCh38.p12 chr7: 144,142,267-159,335,973	CRYGN, GIMAP1, 264 more genes
nsv3918396	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 144,578,280-158,821,317 , GRCh37 chr7: 144,947,347-159,128,556 , GRCh38 chr7: 145,250,254-159,335,866	CRYGN, RN7SL845P, 239 more genes
nsv3924350	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 145,397,037-159,089,306 , GRCh38 chr7: 145,699,944-159,296,617 , NCBI36 chr7: 145,027,970-158,782,067	CRYGN, LOC107986750, 237 more genes
nsv4675268	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 145,962,558-159,119,707 , GRCh38.p12 chr7: 146,265,466-159,327,017	CRYGN, ABCB8, 237 more genes
nsv3923268	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 146,112,671-158,821,424 , GRCh37.p13 chr7: 146,481,738-159,128,663 , GRCh38.p12 chr7: 146,784,646-159,335,973	CRYGN, AOC1, 236 more genes
nsv3923788	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 147,144,002-159,327,017 , NCBI36 chr7: 146,472,027-158,812,468 , GRCh37 chr7: 146,841,094-159,119,707	CRYGN, LOC105375582, 235 more genes
nsv3920858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 146,947,557-159,118,566 , NCBI36 chr7: 146,578,490-158,811,327 , GRCh38 chr7: 147,250,465-159,325,876	CRYGN, RNA5SP250, 233 more genes
nsv3914838	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 145,375,183-157,007,613 , GRCh37 chr7: 145,744,250-157,314,852 , GRCh38 chr7: 146,047,157-157,522,158	CRYGN, WDR86-AS1, 220 more genes
nsv3900730	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 148,238,976-159,126,310 , GRCh38.p12 chr7: 148,541,884-159,333,620	CRYGN, EZH2, 223 more genes
nsv6290897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 148,695,373-159,119,707 , GRCh38.p12 chr7: 148,998,281-159,327,017	CRYGN, TRC-GCA21-1, 209 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 78

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Number of Variants: 20

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